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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: 7-74061138-T-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=7&pos=74061138&ref=T&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "7",
      "pos": 74061138,
      "ref": "T",
      "alt": "C",
      "effect": "splice_region_variant,synonymous_variant",
      "transcript": "NM_001278939.2",
      "consequences": [
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 26,
          "exon_rank_end": null,
          "exon_count": 33,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ELN",
          "gene_hgnc_id": 3327,
          "hgvs_c": "c.1785T>C",
          "hgvs_p": "p.Tyr595Tyr",
          "transcript": "NM_000501.4",
          "protein_id": "NP_000492.2",
          "transcript_support_level": null,
          "aa_start": 595,
          "aa_end": null,
          "aa_length": 724,
          "cds_start": 1785,
          "cds_end": null,
          "cds_length": 2175,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000252034.12",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_000501.4"
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 26,
          "exon_rank_end": null,
          "exon_count": 33,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ELN",
          "gene_hgnc_id": 3327,
          "hgvs_c": "c.1785T>C",
          "hgvs_p": "p.Tyr595Tyr",
          "transcript": "ENST00000252034.12",
          "protein_id": "ENSP00000252034.7",
          "transcript_support_level": 1,
          "aa_start": 595,
          "aa_end": null,
          "aa_length": 724,
          "cds_start": 1785,
          "cds_end": null,
          "cds_length": 2175,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_000501.4",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000252034.12"
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 26,
          "exon_rank_end": null,
          "exon_count": 33,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ELN",
          "gene_hgnc_id": 3327,
          "hgvs_c": "c.1803T>C",
          "hgvs_p": "p.Tyr601Tyr",
          "transcript": "ENST00000380562.8",
          "protein_id": "ENSP00000369936.4",
          "transcript_support_level": 1,
          "aa_start": 601,
          "aa_end": null,
          "aa_length": 730,
          "cds_start": 1803,
          "cds_end": null,
          "cds_length": 2193,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000380562.8"
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 25,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ELN",
          "gene_hgnc_id": 3327,
          "hgvs_c": "c.1755T>C",
          "hgvs_p": "p.Tyr585Tyr",
          "transcript": "ENST00000458204.5",
          "protein_id": "ENSP00000403162.1",
          "transcript_support_level": 1,
          "aa_start": 585,
          "aa_end": null,
          "aa_length": 714,
          "cds_start": 1755,
          "cds_end": null,
          "cds_length": 2145,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000458204.5"
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 26,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ELN",
          "gene_hgnc_id": 3327,
          "hgvs_c": "c.1800T>C",
          "hgvs_p": "p.Tyr600Tyr",
          "transcript": "ENST00000357036.9",
          "protein_id": "ENSP00000349540.5",
          "transcript_support_level": 1,
          "aa_start": 600,
          "aa_end": null,
          "aa_length": 711,
          "cds_start": 1800,
          "cds_end": null,
          "cds_length": 2136,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000357036.9"
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 25,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ELN",
          "gene_hgnc_id": 3327,
          "hgvs_c": "c.1728T>C",
          "hgvs_p": "p.Tyr576Tyr",
          "transcript": "ENST00000380576.9",
          "protein_id": "ENSP00000369950.5",
          "transcript_support_level": 1,
          "aa_start": 576,
          "aa_end": null,
          "aa_length": 705,
          "cds_start": 1728,
          "cds_end": null,
          "cds_length": 2118,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000380576.9"
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 24,
          "exon_rank_end": null,
          "exon_count": 30,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ELN",
          "gene_hgnc_id": 3327,
          "hgvs_c": "c.1698T>C",
          "hgvs_p": "p.Tyr566Tyr",
          "transcript": "ENST00000380575.8",
          "protein_id": "ENSP00000369949.4",
          "transcript_support_level": 1,
          "aa_start": 566,
          "aa_end": null,
          "aa_length": 677,
          "cds_start": 1698,
          "cds_end": null,
          "cds_length": 2034,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000380575.8"
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 23,
          "exon_rank_end": null,
          "exon_count": 29,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ELN",
          "gene_hgnc_id": 3327,
          "hgvs_c": "c.1641T>C",
          "hgvs_p": "p.Tyr547Tyr",
          "transcript": "ENST00000380584.8",
          "protein_id": "ENSP00000369958.4",
          "transcript_support_level": 1,
          "aa_start": 547,
          "aa_end": null,
          "aa_length": 658,
          "cds_start": 1641,
          "cds_end": null,
          "cds_length": 1977,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000380584.8"
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 27,
          "exon_rank_end": null,
          "exon_count": 34,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ELN",
          "gene_hgnc_id": 3327,
          "hgvs_c": "c.1971T>C",
          "hgvs_p": "p.Tyr657Tyr",
          "transcript": "NM_001278939.2",
          "protein_id": "NP_001265868.1",
          "transcript_support_level": null,
          "aa_start": 657,
          "aa_end": null,
          "aa_length": 786,
          "cds_start": 1971,
          "cds_end": null,
          "cds_length": 2361,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001278939.2"
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 27,
          "exon_rank_end": null,
          "exon_count": 34,
          "intron_rank": null,
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          "gene_symbol": "ELN",
          "gene_hgnc_id": 3327,
          "hgvs_c": "c.1971T>C",
          "hgvs_p": "p.Tyr657Tyr",
          "transcript": "ENST00000692049.1",
          "protein_id": "ENSP00000510104.1",
          "transcript_support_level": null,
          "aa_start": 657,
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          "cds_start": 1971,
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          "biotype": "protein_coding",
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        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 26,
          "exon_rank_end": null,
          "exon_count": 33,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ELN",
          "gene_hgnc_id": 3327,
          "hgvs_c": "c.1884T>C",
          "hgvs_p": "p.Tyr628Tyr",
          "transcript": "ENST00000320399.10",
          "protein_id": "ENSP00000313565.6",
          "transcript_support_level": 5,
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          "aa_length": 757,
          "cds_start": 1884,
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          "cdna_start": null,
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        {
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
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          "exon_rank_end": null,
          "exon_count": 34,
          "intron_rank": null,
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          "gene_symbol": "ELN",
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          "hgvs_c": "c.1863T>C",
          "hgvs_p": "p.Tyr621Tyr",
          "transcript": "ENST00000953888.1",
          "protein_id": "ENSP00000623947.1",
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          "cds_start": 1863,
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          "cdna_start": null,
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        },
        {
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          "protein_coding": true,
          "strand": true,
          "consequences": [
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            "synonymous_variant"
          ],
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          "gene_symbol": "ELN",
          "gene_hgnc_id": 3327,
          "hgvs_c": "c.1803T>C",
          "hgvs_p": "p.Tyr601Tyr",
          "transcript": "NM_001278915.2",
          "protein_id": "NP_001265844.1",
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          "aa_end": null,
          "aa_length": 730,
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          "cdna_start": null,
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          "mane_select": null,
          "mane_plus": null,
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          "feature": "NM_001278915.2"
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
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          "protein_coding": true,
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            "synonymous_variant"
          ],
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          "intron_rank": null,
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        {
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          "canonical": false,
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          "strand": true,
          "consequences": [
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          ],
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          "intron_rank": null,
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          "gene_symbol": "ELN",
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          "hgvs_p": "p.Tyr614Tyr",
          "transcript": "ENST00000953850.1",
          "protein_id": "ENSP00000623909.1",
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          "aa_start": 614,
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          "cds_start": 1842,
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          "biotype": "protein_coding",
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        {
          "aa_ref": "Y",
          "aa_alt": "Y",
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          "strand": true,
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          ],
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          "intron_rank": null,
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          "gene_hgnc_id": 3327,
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          "transcript": "ENST00000869853.1",
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          "biotype": "protein_coding",
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        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          "intron_rank": null,
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        {
          "aa_ref": "Y",
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          "strand": true,
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          "intron_rank": null,
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        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
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          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
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          "exon_count": 33,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ELN",
          "gene_hgnc_id": 3327,
          "hgvs_c": "c.1779T>C",
          "hgvs_p": "p.Tyr593Tyr",
          "transcript": "ENST00000953875.1",
          "protein_id": "ENSP00000623934.1",
          "transcript_support_level": null,
          "aa_start": 593,
          "aa_end": null,
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          "cds_start": 1779,
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          "cdna_start": null,
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          "cdna_length": null,
          "mane_select": null,
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          "biotype": "protein_coding",
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        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
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}
For research and educational, non-commercial use only. Not for clinical or diagnostic use. GeneBe does not provide medical advice. Data use for AI modeling is prohibited: if used, the cost is $0.001 per byte of downloaded uncompressed data.