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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: 11-17393034-C-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=11&pos=17393034&ref=C&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "11",
      "pos": 17393034,
      "ref": "C",
      "alt": "A",
      "effect": "missense_variant",
      "transcript": "ENST00000389817.8",
      "consequences": [
        {
          "aa_ref": "R",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 39,
          "exon_rank_end": null,
          "exon_count": 39,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ABCC8",
          "gene_hgnc_id": 59,
          "hgvs_c": "c.4703G>T",
          "hgvs_p": "p.Arg1568Leu",
          "transcript": "NM_000352.6",
          "protein_id": "NP_000343.2",
          "transcript_support_level": null,
          "aa_start": 1568,
          "aa_end": null,
          "aa_length": 1581,
          "cds_start": 4703,
          "cds_end": null,
          "cds_length": 4746,
          "cdna_start": 4772,
          "cdna_end": null,
          "cdna_length": 4921,
          "mane_select": "ENST00000389817.8",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "L",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 39,
          "exon_rank_end": null,
          "exon_count": 39,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ABCC8",
          "gene_hgnc_id": 59,
          "hgvs_c": "c.4703G>T",
          "hgvs_p": "p.Arg1568Leu",
          "transcript": "ENST00000389817.8",
          "protein_id": "ENSP00000374467.4",
          "transcript_support_level": 1,
          "aa_start": 1568,
          "aa_end": null,
          "aa_length": 1581,
          "cds_start": 4703,
          "cds_end": null,
          "cds_length": 4746,
          "cdna_start": 4772,
          "cdna_end": null,
          "cdna_length": 4921,
          "mane_select": "NM_000352.6",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 39,
          "exon_rank_end": null,
          "exon_count": 39,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ABCC8",
          "gene_hgnc_id": 59,
          "hgvs_c": "c.4769G>T",
          "hgvs_p": "p.Arg1590Leu",
          "transcript": "NM_001351295.2",
          "protein_id": "NP_001338224.1",
          "transcript_support_level": null,
          "aa_start": 1590,
          "aa_end": null,
          "aa_length": 1603,
          "cds_start": 4769,
          "cds_end": null,
          "cds_length": 4812,
          "cdna_start": 4838,
          "cdna_end": null,
          "cdna_length": 5374,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 39,
          "exon_rank_end": null,
          "exon_count": 39,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ABCC8",
          "gene_hgnc_id": 59,
          "hgvs_c": "c.4769G>T",
          "hgvs_p": "p.Arg1590Leu",
          "transcript": "ENST00000644772.1",
          "protein_id": "ENSP00000494321.1",
          "transcript_support_level": null,
          "aa_start": 1590,
          "aa_end": null,
          "aa_length": 1603,
          "cds_start": 4769,
          "cds_end": null,
          "cds_length": 4812,
          "cdna_start": 4800,
          "cdna_end": null,
          "cdna_length": 5336,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 39,
          "exon_rank_end": null,
          "exon_count": 39,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ABCC8",
          "gene_hgnc_id": 59,
          "hgvs_c": "c.4706G>T",
          "hgvs_p": "p.Arg1569Leu",
          "transcript": "NM_001287174.3",
          "protein_id": "NP_001274103.1",
          "transcript_support_level": null,
          "aa_start": 1569,
          "aa_end": null,
          "aa_length": 1582,
          "cds_start": 4706,
          "cds_end": null,
          "cds_length": 4749,
          "cdna_start": 4775,
          "cdna_end": null,
          "cdna_length": 4924,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 39,
          "exon_rank_end": null,
          "exon_count": 39,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ABCC8",
          "gene_hgnc_id": 59,
          "hgvs_c": "c.4706G>T",
          "hgvs_p": "p.Arg1569Leu",
          "transcript": "ENST00000302539.9",
          "protein_id": "ENSP00000303960.4",
          "transcript_support_level": 5,
          "aa_start": 1569,
          "aa_end": null,
          "aa_length": 1582,
          "cds_start": 4706,
          "cds_end": null,
          "cds_length": 4749,
          "cdna_start": 4775,
          "cdna_end": null,
          "cdna_length": 4924,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 39,
          "exon_rank_end": null,
          "exon_count": 39,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ABCC8",
          "gene_hgnc_id": 59,
          "hgvs_c": "c.4703G>T",
          "hgvs_p": "p.Arg1568Leu",
          "transcript": "NM_001351296.2",
          "protein_id": "NP_001338225.1",
          "transcript_support_level": null,
          "aa_start": 1568,
          "aa_end": null,
          "aa_length": 1581,
          "cds_start": 4703,
          "cds_end": null,
          "cds_length": 4746,
          "cdna_start": 4772,
          "cdna_end": null,
          "cdna_length": 5308,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 39,
          "exon_rank_end": null,
          "exon_count": 39,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ABCC8",
          "gene_hgnc_id": 59,
          "hgvs_c": "c.4703G>T",
          "hgvs_p": "p.Arg1568Leu",
          "transcript": "ENST00000643260.1",
          "protein_id": "ENSP00000494450.1",
          "transcript_support_level": null,
          "aa_start": 1568,
          "aa_end": null,
          "aa_length": 1581,
          "cds_start": 4703,
          "cds_end": null,
          "cds_length": 4746,
          "cdna_start": 4772,
          "cdna_end": null,
          "cdna_length": 4903,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 39,
          "exon_rank_end": null,
          "exon_count": 39,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ABCC8",
          "gene_hgnc_id": 59,
          "hgvs_c": "c.4700G>T",
          "hgvs_p": "p.Arg1567Leu",
          "transcript": "NM_001351297.2",
          "protein_id": "NP_001338226.1",
          "transcript_support_level": null,
          "aa_start": 1567,
          "aa_end": null,
          "aa_length": 1580,
          "cds_start": 4700,
          "cds_end": null,
          "cds_length": 4743,
          "cdna_start": 4769,
          "cdna_end": null,
          "cdna_length": 5305,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 39,
          "exon_rank_end": null,
          "exon_count": 39,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ABCC8",
          "gene_hgnc_id": 59,
          "hgvs_c": "c.4700G>T",
          "hgvs_p": "p.Arg1567Leu",
          "transcript": "ENST00000642271.1",
          "protein_id": "ENSP00000493749.1",
          "transcript_support_level": null,
          "aa_start": 1567,
          "aa_end": null,
          "aa_length": 1580,
          "cds_start": 4700,
          "cds_end": null,
          "cds_length": 4743,
          "cdna_start": 4735,
          "cdna_end": null,
          "cdna_length": 4866,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 39,
          "exon_rank_end": null,
          "exon_count": 39,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ABCC8",
          "gene_hgnc_id": 59,
          "hgvs_c": "c.4670G>T",
          "hgvs_p": "p.Arg1557Leu",
          "transcript": "ENST00000646902.1",
          "protein_id": "ENSP00000494101.1",
          "transcript_support_level": null,
          "aa_start": 1557,
          "aa_end": null,
          "aa_length": 1570,
          "cds_start": 4670,
          "cds_end": null,
          "cds_length": 4713,
          "cdna_start": 4738,
          "cdna_end": null,
          "cdna_length": 4874,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 38,
          "exon_rank_end": null,
          "exon_count": 38,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ABCC8",
          "gene_hgnc_id": 59,
          "hgvs_c": "c.4586G>T",
          "hgvs_p": "p.Arg1529Leu",
          "transcript": "ENST00000683136.1",
          "protein_id": "ENSP00000507768.1",
          "transcript_support_level": null,
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          "aa_end": null,
          "aa_length": 1542,
          "cds_start": 4586,
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          "cdna_start": 4682,
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          "cdna_length": 4819,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 38,
          "exon_rank_end": null,
          "exon_count": 38,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ABCC8",
          "gene_hgnc_id": 59,
          "hgvs_c": "c.4544G>T",
          "hgvs_p": "p.Arg1515Leu",
          "transcript": "ENST00000684571.1",
          "protein_id": "ENSP00000506935.1",
          "transcript_support_level": null,
          "aa_start": 1515,
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          "aa_length": 1528,
          "cds_start": 4544,
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          "cdna_start": 4585,
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          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 37,
          "exon_rank_end": null,
          "exon_count": 37,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ABCC8",
          "gene_hgnc_id": 59,
          "hgvs_c": "c.4454G>T",
          "hgvs_p": "p.Arg1485Leu",
          "transcript": "ENST00000647015.1",
          "protein_id": "ENSP00000495389.1",
          "transcript_support_level": null,
          "aa_start": 1485,
          "aa_end": null,
          "aa_length": 1498,
          "cds_start": 4454,
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          "cds_length": 4497,
          "cdna_start": 4522,
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          "cdna_length": 4642,
          "mane_select": null,
          "mane_plus": null,
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          "feature": null
        },
        {
          "aa_ref": "R",
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          "canonical": false,
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          "consequences": [
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          ],
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          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ABCC8",
          "gene_hgnc_id": 59,
          "hgvs_c": "c.2756G>T",
          "hgvs_p": "p.Arg919Leu",
          "transcript": "ENST00000642579.1",
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          "transcript_support_level": null,
          "aa_start": 919,
          "aa_end": null,
          "aa_length": 932,
          "cds_start": 2756,
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          "cdna_start": 2757,
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          "cdna_length": 2893,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ABCC8",
          "gene_hgnc_id": 59,
          "hgvs_c": "c.1292G>T",
          "hgvs_p": "p.Arg431Leu",
          "transcript": "ENST00000528374.2",
          "protein_id": "ENSP00000433638.2",
          "transcript_support_level": 5,
          "aa_start": 431,
          "aa_end": null,
          "aa_length": 444,
          "cds_start": 1292,
          "cds_end": null,
          "cds_length": 1335,
          "cdna_start": 1294,
          "cdna_end": null,
          "cdna_length": 1443,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 34,
          "exon_rank_end": null,
          "exon_count": 34,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ABCC8",
          "gene_hgnc_id": 59,
          "hgvs_c": "n.4304G>T",
          "hgvs_p": null,
          "transcript": "ENST00000524561.2",
          "protein_id": null,
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
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          "cdna_length": 4441,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ABCC8",
          "gene_hgnc_id": 59,
          "hgvs_c": "n.638G>T",
          "hgvs_p": null,
          "transcript": "ENST00000526037.6",
          "protein_id": null,
          "transcript_support_level": 3,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
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          "cdna_start": null,
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          "cdna_length": 775,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ABCC8",
          "gene_hgnc_id": 59,
          "hgvs_c": "n.*390G>T",
          "hgvs_p": null,
          "transcript": "ENST00000526168.5",
          "protein_id": "ENSP00000437233.1",
          "transcript_support_level": 2,
          "aa_start": null,
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          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
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          "cdna_length": 537,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 26,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ABCC8",
          "gene_hgnc_id": 59,
          "hgvs_c": "n.3042G>T",
          "hgvs_p": null,
          "transcript": "ENST00000529967.6",
          "protein_id": null,
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3179,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ABCC8",
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