# Lookup by stable ID Ensembl Genomics (Genes, Variants,

**Use case:** 

Extract Ensembl Genomics (Genes, Variants, Sequences) data filtered by Lookup by stable ID. Export structured results ready for analysis, lead generation, or

## Input

```json
{
  "maxItems": 10,
  "mode": "lookupId",
  "species": "homo_sapiens",
  "symbols": [
    "BRCA2",
    "TP53",
    "EGFR",
    "MYC",
    "KRAS"
  ]
}
```

## Output

```json
{
  "stableId": {
    "label": "Stable ID",
    "format": "text"
  },
  "displayName": {
    "label": "Display Name",
    "format": "text"
  },
  "objectType": {
    "label": "Type",
    "format": "text"
  },
  "biotype": {
    "label": "Biotype",
    "format": "text"
  },
  "species": {
    "label": "Species",
    "format": "text"
  },
  "chromosome": {
    "label": "Chr",
    "format": "text"
  },
  "start": {
    "label": "Start",
    "format": "number"
  },
  "end": {
    "label": "End",
    "format": "number"
  },
  "strand": {
    "label": "Strand",
    "format": "number"
  },
  "assemblyName": {
    "label": "Assembly",
    "format": "text"
  },
  "description": {
    "label": "Description",
    "format": "text"
  },
  "canonicalTranscript": {
    "label": "Canonical Transcript",
    "format": "text"
  },
  "source": {
    "label": "Source",
    "format": "text"
  },
  "logicName": {
    "label": "Logic",
    "format": "text"
  },
  "molecule": {
    "label": "Molecule",
    "format": "text"
  },
  "sequenceLength": {
    "label": "Seq Length",
    "format": "number"
  },
  "sequence": {
    "label": "Sequence",
    "format": "text"
  },
  "variantName": {
    "label": "Variant",
    "format": "text"
  },
  "varClass": {
    "label": "Var Class",
    "format": "text"
  },
  "minorAllele": {
    "label": "Minor Allele",
    "format": "text"
  },
  "minorAlleleFreq": {
    "label": "MAF",
    "format": "number"
  },
  "ancestralAllele": {
    "label": "Ancestral",
    "format": "text"
  },
  "alleleString": {
    "label": "Alleles",
    "format": "text"
  },
  "mostSevereConsequence": {
    "label": "Consequence",
    "format": "text"
  },
  "mappings": {
    "label": "Mappings",
    "format": "object"
  },
  "evidence": {
    "label": "Evidence",
    "format": "object"
  },
  "synonyms": {
    "label": "Synonyms",
    "format": "object"
  },
  "mode": {
    "label": "Mode",
    "format": "text"
  },
  "query": {
    "label": "Query",
    "format": "text"
  },
  "scrapedAt": {
    "label": "Collected",
    "format": "date"
  },
  "error": {
    "label": "Error",
    "format": "text"
  }
}
```

## About this Actor

This example demonstrates how to use [Ensembl Genomics Scraper (Genes, Variants, Sequences)](https://apify.com/parseforge/ensembl-genomics-scraper) with a specific input configuration. Visit the [Actor detail page](https://apify.com/parseforge/ensembl-genomics-scraper) to learn more, explore other use cases, and run it yourself.