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GeneBe API Showcase

This page demonstrates how to use the GeneBe API to query variant information. The API provides programmatic access to genomic annotations and variant data.

API presented here should be used for checking single variants. If you want to check many variants at once, please use other API endpoints that you will find in the documentation.

Documentation & Advanced Usage

Complete API documentation:docs.genebe.net/docs/api/overview/

Interactive endpoint tester:api.genebe.net/cloud/gb-api-doc/swagger-ui/

Python client for pandas:pypi.org/project/genebe/

Java CLI for VCF files:github.com/pstawinski/genebe-cli

All tools documented at:docs.genebe.net

API Request Examples for Variant: 7-148807679-A-G (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=7&pos=148807679&ref=A&alt=G&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "7",
      "pos": 148807679,
      "ref": "A",
      "alt": "G",
      "effect": "synonymous_variant",
      "transcript": "NM_004456.5",
      "consequences": [
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "EZH2",
          "gene_hgnc_id": 3527,
          "hgvs_c": "c.2223T>C",
          "hgvs_p": "p.Tyr741Tyr",
          "transcript": "NM_004456.5",
          "protein_id": "NP_004447.2",
          "transcript_support_level": null,
          "aa_start": 741,
          "aa_end": null,
          "aa_length": 751,
          "cds_start": 2223,
          "cds_end": null,
          "cds_length": 2256,
          "cdna_start": 2358,
          "cdna_end": null,
          "cdna_length": 2654,
          "mane_select": "ENST00000320356.7",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "EZH2",
          "gene_hgnc_id": 3527,
          "hgvs_c": "c.2223T>C",
          "hgvs_p": "p.Tyr741Tyr",
          "transcript": "ENST00000320356.7",
          "protein_id": "ENSP00000320147.2",
          "transcript_support_level": 1,
          "aa_start": 741,
          "aa_end": null,
          "aa_length": 751,
          "cds_start": 2223,
          "cds_end": null,
          "cds_length": 2256,
          "cdna_start": 2358,
          "cdna_end": null,
          "cdna_length": 2654,
          "mane_select": "NM_004456.5",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "EZH2",
          "gene_hgnc_id": 3527,
          "hgvs_c": "c.2208T>C",
          "hgvs_p": "p.Tyr736Tyr",
          "transcript": "ENST00000460911.5",
          "protein_id": "ENSP00000419711.1",
          "transcript_support_level": 1,
          "aa_start": 736,
          "aa_end": null,
          "aa_length": 746,
          "cds_start": 2208,
          "cds_end": null,
          "cds_length": 2241,
          "cdna_start": 2297,
          "cdna_end": null,
          "cdna_length": 2591,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "EZH2",
          "gene_hgnc_id": 3527,
          "hgvs_c": "c.2091T>C",
          "hgvs_p": "p.Tyr697Tyr",
          "transcript": "ENST00000350995.6",
          "protein_id": "ENSP00000223193.2",
          "transcript_support_level": 1,
          "aa_start": 697,
          "aa_end": null,
          "aa_length": 707,
          "cds_start": 2091,
          "cds_end": null,
          "cds_length": 2124,
          "cdna_start": 2183,
          "cdna_end": null,
          "cdna_length": 2477,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "EZH2",
          "gene_hgnc_id": 3527,
          "hgvs_c": "c.2208T>C",
          "hgvs_p": "p.Tyr736Tyr",
          "transcript": "NM_001203247.2",
          "protein_id": "NP_001190176.1",
          "transcript_support_level": null,
          "aa_start": 736,
          "aa_end": null,
          "aa_length": 746,
          "cds_start": 2208,
          "cds_end": null,
          "cds_length": 2241,
          "cdna_start": 2343,
          "cdna_end": null,
          "cdna_length": 2639,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "EZH2",
          "gene_hgnc_id": 3527,
          "hgvs_c": "c.2181T>C",
          "hgvs_p": "p.Tyr727Tyr",
          "transcript": "NM_001203248.2",
          "protein_id": "NP_001190177.1",
          "transcript_support_level": null,
          "aa_start": 727,
          "aa_end": null,
          "aa_length": 737,
          "cds_start": 2181,
          "cds_end": null,
          "cds_length": 2214,
          "cdna_start": 2316,
          "cdna_end": null,
          "cdna_length": 2612,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "EZH2",
          "gene_hgnc_id": 3527,
          "hgvs_c": "c.2181T>C",
          "hgvs_p": "p.Tyr727Tyr",
          "transcript": "ENST00000483967.5",
          "protein_id": "ENSP00000419856.1",
          "transcript_support_level": 2,
          "aa_start": 727,
          "aa_end": null,
          "aa_length": 737,
          "cds_start": 2181,
          "cds_end": null,
          "cds_length": 2214,
          "cdna_start": 2312,
          "cdna_end": null,
          "cdna_length": 2466,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "EZH2",
          "gene_hgnc_id": 3527,
          "hgvs_c": "c.2091T>C",
          "hgvs_p": "p.Tyr697Tyr",
          "transcript": "NM_152998.3",
          "protein_id": "NP_694543.1",
          "transcript_support_level": null,
          "aa_start": 697,
          "aa_end": null,
          "aa_length": 707,
          "cds_start": 2091,
          "cds_end": null,
          "cds_length": 2124,
          "cdna_start": 2226,
          "cdna_end": null,
          "cdna_length": 2522,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "EZH2",
          "gene_hgnc_id": 3527,
          "hgvs_c": "c.2055T>C",
          "hgvs_p": "p.Tyr685Tyr",
          "transcript": "NM_001203249.2",
          "protein_id": "NP_001190178.1",
          "transcript_support_level": null,
          "aa_start": 685,
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          "cds_start": 2055,
          "cds_end": null,
          "cds_length": 2088,
          "cdna_start": 2351,
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          "mane_select": null,
          "mane_plus": null,
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        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
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          "gene_symbol": "EZH2",
          "gene_hgnc_id": 3527,
          "hgvs_c": "c.2055T>C",
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          "transcript": "ENST00000476773.5",
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        {
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          "intron_rank": null,
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        {
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        {
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          "gene_symbol": "EZH2",
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          "transcript": "XM_005249963.5",
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        },
        {
          "aa_ref": "Y",
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          "consequences": [
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          ],
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      "clinvar_classification": "Likely benign",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "LB:1",
      "phenotype_combined": "Weaver syndrome",
      "pathogenicity_classification_combined": "Likely benign",
      "custom_annotations": null
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  "message": null
}