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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: 2-232768405-G-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=232768405&ref=G&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "2",
      "pos": 232768405,
      "ref": "G",
      "alt": "C",
      "effect": "missense_variant",
      "transcript": "NM_002242.4",
      "consequences": [
        {
          "aa_ref": "P",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KCNJ13",
          "gene_hgnc_id": 6259,
          "hgvs_c": "c.869C>G",
          "hgvs_p": "p.Pro290Arg",
          "transcript": "NM_002242.4",
          "protein_id": "NP_002233.2",
          "transcript_support_level": null,
          "aa_start": 290,
          "aa_end": null,
          "aa_length": 360,
          "cds_start": 869,
          "cds_end": null,
          "cds_length": 1083,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000233826.4",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_002242.4"
        },
        {
          "aa_ref": "P",
          "aa_alt": "R",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KCNJ13",
          "gene_hgnc_id": 6259,
          "hgvs_c": "c.869C>G",
          "hgvs_p": "p.Pro290Arg",
          "transcript": "ENST00000233826.4",
          "protein_id": "ENSP00000233826.3",
          "transcript_support_level": 1,
          "aa_start": 290,
          "aa_end": null,
          "aa_length": 360,
          "cds_start": 869,
          "cds_end": null,
          "cds_length": 1083,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_002242.4",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000233826.4"
        },
        {
          "aa_ref": "P",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 2,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KCNJ13",
          "gene_hgnc_id": 6259,
          "hgvs_c": "c.869C>G",
          "hgvs_p": "p.Pro290Arg",
          "transcript": "ENST00000410029.1",
          "protein_id": "ENSP00000386251.1",
          "transcript_support_level": 1,
          "aa_start": 290,
          "aa_end": null,
          "aa_length": 360,
          "cds_start": 869,
          "cds_end": null,
          "cds_length": 1083,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000410029.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 29,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "GIGYF2",
          "gene_hgnc_id": 11960,
          "hgvs_c": "c.532+6969G>C",
          "hgvs_p": null,
          "transcript": "NM_001103146.3",
          "protein_id": "NP_001096616.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1299,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3900,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000373563.9",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001103146.3"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 29,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "GIGYF2",
          "gene_hgnc_id": 11960,
          "hgvs_c": "c.532+6969G>C",
          "hgvs_p": null,
          "transcript": "ENST00000373563.9",
          "protein_id": "ENSP00000362664.5",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1299,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3900,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_001103146.3",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000373563.9"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 31,
          "intron_rank": 9,
          "intron_rank_end": null,
          "gene_symbol": "GIGYF2",
          "gene_hgnc_id": 11960,
          "hgvs_c": "c.532+6969G>C",
          "hgvs_p": null,
          "transcript": "ENST00000409451.7",
          "protein_id": "ENSP00000387170.3",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1320,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3963,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000409451.7"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 31,
          "intron_rank": 10,
          "intron_rank_end": null,
          "gene_symbol": "GIGYF2",
          "gene_hgnc_id": 11960,
          "hgvs_c": "c.532+6969G>C",
          "hgvs_p": null,
          "transcript": "ENST00000409547.5",
          "protein_id": "ENSP00000386537.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1299,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3900,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000409547.5"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "GIGYF2",
          "gene_hgnc_id": 11960,
          "hgvs_c": "c.532+6969G>C",
          "hgvs_p": null,
          "transcript": "ENST00000409196.7",
          "protein_id": "ENSP00000387070.3",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1293,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3882,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000409196.7"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "GIGYF2",
          "gene_hgnc_id": 11960,
          "hgvs_c": "c.532+6969G>C",
          "hgvs_p": null,
          "transcript": "ENST00000440945.5",
          "protein_id": "ENSP00000410297.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 835,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2508,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000440945.5"
        },
        {
          "aa_ref": "P",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KCNJ13",
          "gene_hgnc_id": 6259,
          "hgvs_c": "c.629C>G",
          "hgvs_p": "p.Pro210Arg",
          "transcript": "NM_001172417.1",
          "protein_id": "NP_001165888.1",
          "transcript_support_level": null,
          "aa_start": 210,
          "aa_end": null,
          "aa_length": 280,
          "cds_start": 629,
          "cds_end": null,
          "cds_length": 843,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001172417.1"
        },
        {
          "aa_ref": "P",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KCNJ13",
          "gene_hgnc_id": 6259,
          "hgvs_c": "c.869C>G",
          "hgvs_p": "p.Pro290Arg",
          "transcript": "XM_047444253.1",
          "protein_id": "XP_047300209.1",
          "transcript_support_level": null,
          "aa_start": 290,
          "aa_end": null,
          "aa_length": 360,
          "cds_start": 869,
          "cds_end": null,
          "cds_length": 1083,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "XM_047444253.1"
        },
        {
          "aa_ref": "G",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant",
            "splice_region_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "GIGYF2",
          "gene_hgnc_id": 11960,
          "hgvs_c": "c.13G>C",
          "hgvs_p": "p.Gly5Arg",
          "transcript": "ENST00000677450.1",
          "protein_id": "ENSP00000503420.1",
          "transcript_support_level": null,
          "aa_start": 5,
          "aa_end": null,
          "aa_length": 1126,
          "cds_start": 13,
          "cds_end": null,
          "cds_length": 3381,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000677450.1"
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 2,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KCNJ13",
          "gene_hgnc_id": 6259,
          "hgvs_c": "c.405C>G",
          "hgvs_p": "p.Thr135Thr",
          "transcript": "ENST00000444142.1",
          "protein_id": "ENSP00000416896.1",
          "transcript_support_level": 5,
          "aa_start": 135,
          "aa_end": null,
          "aa_length": 136,
          "cds_start": 405,
          "cds_end": null,
          "cds_length": 411,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000444142.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KCNJ13",
          "gene_hgnc_id": 6259,
          "hgvs_c": "c.*348C>G",
          "hgvs_p": null,
          "transcript": "NM_001172416.1",
          "protein_id": "NP_001165887.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 94,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 285,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001172416.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KCNJ13",
          "gene_hgnc_id": 6259,
          "hgvs_c": "c.*348C>G",
          "hgvs_p": null,
          "transcript": "ENST00000409779.1",
          "protein_id": "ENSP00000386408.1",
          "transcript_support_level": 2,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 94,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 285,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000409779.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 31,
          "intron_rank": 9,
          "intron_rank_end": null,
          "gene_symbol": "GIGYF2",
          "gene_hgnc_id": 11960,
          "hgvs_c": "c.532+6969G>C",
          "hgvs_p": null,
          "transcript": "ENST00000409480.5",
          "protein_id": "ENSP00000386765.1",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1321,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3966,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000409480.5"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 30,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "GIGYF2",
          "gene_hgnc_id": 11960,
          "hgvs_c": "c.532+6969G>C",
          "hgvs_p": null,
          "transcript": "ENST00000629305.2",
          "protein_id": "ENSP00000487548.1",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1321,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3966,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000629305.2"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 31,
          "intron_rank": 9,
          "intron_rank_end": null,
          "gene_symbol": "GIGYF2",
          "gene_hgnc_id": 11960,
          "hgvs_c": "c.532+6969G>C",
          "hgvs_p": null,
          "transcript": "NM_001103147.2",
          "protein_id": "NP_001096617.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1320,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3963,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001103147.2"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 31,
          "intron_rank": 10,
          "intron_rank_end": null,
          "gene_symbol": "GIGYF2",
          "gene_hgnc_id": 11960,
          "hgvs_c": "c.532+6969G>C",
          "hgvs_p": null,
          "transcript": "NM_015575.4",
          "protein_id": "NP_056390.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1299,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3900,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_015575.4"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "GIGYF2",
          "gene_hgnc_id": 11960,
          "hgvs_c": "c.532+6969G>C",
          "hgvs_p": null,
          "transcript": "ENST00000869690.1",
          "protein_id": "ENSP00000539749.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1299,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3900,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000869690.1"
        },
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}