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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: 6-26407828-C-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=6&pos=26407828&ref=C&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "6",
      "pos": 26407828,
      "ref": "C",
      "alt": "T",
      "effect": "splice_region_variant,synonymous_variant",
      "transcript": "NM_001145008.2",
      "consequences": [
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BTN3A1",
          "gene_hgnc_id": 1138,
          "hgvs_c": "c.591C>T",
          "hgvs_p": "p.Asp197Asp",
          "transcript": "NM_007048.6",
          "protein_id": "NP_008979.3",
          "transcript_support_level": null,
          "aa_start": 197,
          "aa_end": null,
          "aa_length": 513,
          "cds_start": 591,
          "cds_end": null,
          "cds_length": 1542,
          "cdna_start": 921,
          "cdna_end": null,
          "cdna_length": 3388,
          "mane_select": "ENST00000289361.11",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_007048.6"
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BTN3A1",
          "gene_hgnc_id": 1138,
          "hgvs_c": "c.591C>T",
          "hgvs_p": "p.Asp197Asp",
          "transcript": "ENST00000289361.11",
          "protein_id": "ENSP00000289361.6",
          "transcript_support_level": 1,
          "aa_start": 197,
          "aa_end": null,
          "aa_length": 513,
          "cds_start": 591,
          "cds_end": null,
          "cds_length": 1542,
          "cdna_start": 921,
          "cdna_end": null,
          "cdna_length": 3388,
          "mane_select": "NM_007048.6",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000289361.11"
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BTN3A1",
          "gene_hgnc_id": 1138,
          "hgvs_c": "c.591C>T",
          "hgvs_p": "p.Asp197Asp",
          "transcript": "ENST00000476549.6",
          "protein_id": "ENSP00000420010.2",
          "transcript_support_level": 1,
          "aa_start": 197,
          "aa_end": null,
          "aa_length": 352,
          "cds_start": 591,
          "cds_end": null,
          "cds_length": 1059,
          "cdna_start": 789,
          "cdna_end": null,
          "cdna_length": 1758,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000476549.6"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "5_prime_UTR_premature_start_codon_gain_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BTN3A1",
          "gene_hgnc_id": 1138,
          "hgvs_c": "c.-895C>T",
          "hgvs_p": null,
          "transcript": "XM_047418127.1",
          "protein_id": "XP_047274083.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 321,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 966,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4942,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "XM_047418127.1"
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BTN3A1",
          "gene_hgnc_id": 1138,
          "hgvs_c": "c.591C>T",
          "hgvs_p": "p.Asp197Asp",
          "transcript": "ENST00000850859.1",
          "protein_id": "ENSP00000520946.1",
          "transcript_support_level": null,
          "aa_start": 197,
          "aa_end": null,
          "aa_length": 513,
          "cds_start": 591,
          "cds_end": null,
          "cds_length": 1542,
          "cdna_start": 921,
          "cdna_end": null,
          "cdna_length": 3396,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000850859.1"
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BTN3A1",
          "gene_hgnc_id": 1138,
          "hgvs_c": "c.591C>T",
          "hgvs_p": "p.Asp197Asp",
          "transcript": "ENST00000865809.1",
          "protein_id": "ENSP00000535868.1",
          "transcript_support_level": null,
          "aa_start": 197,
          "aa_end": null,
          "aa_length": 513,
          "cds_start": 591,
          "cds_end": null,
          "cds_length": 1542,
          "cdna_start": 776,
          "cdna_end": null,
          "cdna_length": 3239,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000865809.1"
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BTN3A1",
          "gene_hgnc_id": 1138,
          "hgvs_c": "c.591C>T",
          "hgvs_p": "p.Asp197Asp",
          "transcript": "ENST00000865808.1",
          "protein_id": "ENSP00000535867.1",
          "transcript_support_level": null,
          "aa_start": 197,
          "aa_end": null,
          "aa_length": 506,
          "cds_start": 591,
          "cds_end": null,
          "cds_length": 1521,
          "cdna_start": 959,
          "cdna_end": null,
          "cdna_length": 3413,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000865808.1"
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BTN3A1",
          "gene_hgnc_id": 1138,
          "hgvs_c": "c.435C>T",
          "hgvs_p": "p.Asp145Asp",
          "transcript": "NM_001145008.2",
          "protein_id": "NP_001138480.1",
          "transcript_support_level": null,
          "aa_start": 145,
          "aa_end": null,
          "aa_length": 461,
          "cds_start": 435,
          "cds_end": null,
          "cds_length": 1386,
          "cdna_start": 765,
          "cdna_end": null,
          "cdna_length": 3232,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001145008.2"
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BTN3A1",
          "gene_hgnc_id": 1138,
          "hgvs_c": "c.435C>T",
          "hgvs_p": "p.Asp145Asp",
          "transcript": "ENST00000414912.2",
          "protein_id": "ENSP00000406667.2",
          "transcript_support_level": 2,
          "aa_start": 145,
          "aa_end": null,
          "aa_length": 461,
          "cds_start": 435,
          "cds_end": null,
          "cds_length": 1386,
          "cdna_start": 745,
          "cdna_end": null,
          "cdna_length": 2077,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000414912.2"
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BTN3A1",
          "gene_hgnc_id": 1138,
          "hgvs_c": "c.435C>T",
          "hgvs_p": "p.Asp145Asp",
          "transcript": "ENST00000865812.1",
          "protein_id": "ENSP00000535871.1",
          "transcript_support_level": null,
          "aa_start": 145,
          "aa_end": null,
          "aa_length": 461,
          "cds_start": 435,
          "cds_end": null,
          "cds_length": 1386,
          "cdna_start": 568,
          "cdna_end": null,
          "cdna_length": 3030,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000865812.1"
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BTN3A1",
          "gene_hgnc_id": 1138,
          "hgvs_c": "c.435C>T",
          "hgvs_p": "p.Asp145Asp",
          "transcript": "ENST00000865811.1",
          "protein_id": "ENSP00000535870.1",
          "transcript_support_level": null,
          "aa_start": 145,
          "aa_end": null,
          "aa_length": 454,
          "cds_start": 435,
          "cds_end": null,
          "cds_length": 1365,
          "cdna_start": 728,
          "cdna_end": null,
          "cdna_length": 3182,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000865811.1"
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BTN3A1",
          "gene_hgnc_id": 1138,
          "hgvs_c": "c.591C>T",
          "hgvs_p": "p.Asp197Asp",
          "transcript": "NM_001145009.2",
          "protein_id": "NP_001138481.1",
          "transcript_support_level": null,
          "aa_start": 197,
          "aa_end": null,
          "aa_length": 378,
          "cds_start": 591,
          "cds_end": null,
          "cds_length": 1137,
          "cdna_start": 921,
          "cdna_end": null,
          "cdna_length": 4145,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001145009.2"
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BTN3A1",
          "gene_hgnc_id": 1138,
          "hgvs_c": "c.591C>T",
          "hgvs_p": "p.Asp197Asp",
          "transcript": "ENST00000425234.6",
          "protein_id": "ENSP00000396684.2",
          "transcript_support_level": 2,
          "aa_start": 197,
          "aa_end": null,
          "aa_length": 378,
          "cds_start": 591,
          "cds_end": null,
          "cds_length": 1137,
          "cdna_start": 946,
          "cdna_end": null,
          "cdna_length": 1882,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000425234.6"
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BTN3A1",
          "gene_hgnc_id": 1138,
          "hgvs_c": "c.591C>T",
          "hgvs_p": "p.Asp197Asp",
          "transcript": "NM_194441.3",
          "protein_id": "NP_919423.1",
          "transcript_support_level": null,
          "aa_start": 197,
          "aa_end": null,
          "aa_length": 352,
          "cds_start": 591,
          "cds_end": null,
          "cds_length": 1059,
          "cdna_start": 751,
          "cdna_end": null,
          "cdna_length": 3682,
          "mane_select": null,
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          "biotype": "protein_coding",
          "feature": "NM_194441.3"
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BTN3A1",
          "gene_hgnc_id": 1138,
          "hgvs_c": "c.591C>T",
          "hgvs_p": "p.Asp197Asp",
          "transcript": "XM_047418120.1",
          "protein_id": "XP_047274076.1",
          "transcript_support_level": null,
          "aa_start": 197,
          "aa_end": null,
          "aa_length": 513,
          "cds_start": 591,
          "cds_end": null,
          "cds_length": 1542,
          "cdna_start": 2158,
          "cdna_end": null,
          "cdna_length": 4625,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "XM_047418120.1"
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BTN3A1",
          "gene_hgnc_id": 1138,
          "hgvs_c": "c.591C>T",
          "hgvs_p": "p.Asp197Asp",
          "transcript": "XM_047418121.1",
          "protein_id": "XP_047274077.1",
          "transcript_support_level": null,
          "aa_start": 197,
          "aa_end": null,
          "aa_length": 513,
          "cds_start": 591,
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          "cds_length": 1542,
          "cdna_start": 1753,
          "cdna_end": null,
          "cdna_length": 4220,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "XM_047418121.1"
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BTN3A1",
          "gene_hgnc_id": 1138,
          "hgvs_c": "c.591C>T",
          "hgvs_p": "p.Asp197Asp",
          "transcript": "XM_005248833.3",
          "protein_id": "XP_005248890.1",
          "transcript_support_level": null,
          "aa_start": 197,
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          "aa_length": 506,
          "cds_start": 591,
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          "cds_length": 1521,
          "cdna_start": 921,
          "cdna_end": null,
          "cdna_length": 3367,
          "mane_select": null,
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          "biotype": "protein_coding",
          "feature": "XM_005248833.3"
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
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          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BTN3A1",
          "gene_hgnc_id": 1138,
          "hgvs_c": "c.591C>T",
          "hgvs_p": "p.Asp197Asp",
          "transcript": "XM_047418122.1",
          "protein_id": "XP_047274078.1",
          "transcript_support_level": null,
          "aa_start": 197,
          "aa_end": null,
          "aa_length": 506,
          "cds_start": 591,
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          "cds_length": 1521,
          "cdna_start": 2158,
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          "mane_select": null,
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          "biotype": "protein_coding",
          "feature": "XM_047418122.1"
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BTN3A1",
          "gene_hgnc_id": 1138,
          "hgvs_c": "c.591C>T",
          "hgvs_p": "p.Asp197Asp",
          "transcript": "XM_047418123.1",
          "protein_id": "XP_047274079.1",
          "transcript_support_level": null,
          "aa_start": 197,
          "aa_end": null,
          "aa_length": 378,
          "cds_start": 591,
          "cds_end": null,
          "cds_length": 1137,
          "cdna_start": 1753,
          "cdna_end": null,
          "cdna_length": 4977,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "XM_047418123.1"
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BTN3A1",
          "gene_hgnc_id": 1138,
          "hgvs_c": "c.591C>T",
          "hgvs_p": "p.Asp197Asp",
          "transcript": "XM_005248834.5",
          "protein_id": "XP_005248891.1",
          "transcript_support_level": null,
          "aa_start": 197,
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      "clinvar_review_status": "",
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      "custom_annotations": null
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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.