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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: 11-16791013-T-G (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=11&pos=16791013&ref=T&alt=G&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "11",
      "pos": 16791013,
      "ref": "T",
      "alt": "G",
      "effect": "splice_region_variant,synonymous_variant",
      "transcript": "NM_001410960.1",
      "consequences": [
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLEKHA7",
          "gene_hgnc_id": 27049,
          "hgvs_c": "c.2932A>C",
          "hgvs_p": "p.Arg978Arg",
          "transcript": "NM_001329630.2",
          "protein_id": "NP_001316559.1",
          "transcript_support_level": null,
          "aa_start": 978,
          "aa_end": null,
          "aa_length": 1271,
          "cds_start": 2932,
          "cds_end": null,
          "cds_length": 3816,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000531066.6",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001329630.2"
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLEKHA7",
          "gene_hgnc_id": 27049,
          "hgvs_c": "c.2932A>C",
          "hgvs_p": "p.Arg978Arg",
          "transcript": "ENST00000531066.6",
          "protein_id": "ENSP00000435389.1",
          "transcript_support_level": 5,
          "aa_start": 978,
          "aa_end": null,
          "aa_length": 1271,
          "cds_start": 2932,
          "cds_end": null,
          "cds_length": 3816,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_001329630.2",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000531066.6"
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLEKHA7",
          "gene_hgnc_id": 27049,
          "hgvs_c": "c.2932A>C",
          "hgvs_p": "p.Arg978Arg",
          "transcript": "ENST00000355661.7",
          "protein_id": "ENSP00000347883.2",
          "transcript_support_level": 1,
          "aa_start": 978,
          "aa_end": null,
          "aa_length": 1121,
          "cds_start": 2932,
          "cds_end": null,
          "cds_length": 3366,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000355661.7"
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLEKHA7",
          "gene_hgnc_id": 27049,
          "hgvs_c": "c.1825A>C",
          "hgvs_p": "p.Arg609Arg",
          "transcript": "ENST00000530489.5",
          "protein_id": "ENSP00000433467.1",
          "transcript_support_level": 1,
          "aa_start": 609,
          "aa_end": null,
          "aa_length": 752,
          "cds_start": 1825,
          "cds_end": null,
          "cds_length": 2259,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000530489.5"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLEKHA7",
          "gene_hgnc_id": 27049,
          "hgvs_c": "n.331A>C",
          "hgvs_p": null,
          "transcript": "ENST00000332954.8",
          "protein_id": null,
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": null,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "pseudogene",
          "feature": "ENST00000332954.8"
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLEKHA7",
          "gene_hgnc_id": 27049,
          "hgvs_c": "c.2935A>C",
          "hgvs_p": "p.Arg979Arg",
          "transcript": "NM_001410960.1",
          "protein_id": "NP_001397889.1",
          "transcript_support_level": null,
          "aa_start": 979,
          "aa_end": null,
          "aa_length": 1272,
          "cds_start": 2935,
          "cds_end": null,
          "cds_length": 3819,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001410960.1"
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLEKHA7",
          "gene_hgnc_id": 27049,
          "hgvs_c": "c.2935A>C",
          "hgvs_p": "p.Arg979Arg",
          "transcript": "ENST00000698836.1",
          "protein_id": "ENSP00000513972.1",
          "transcript_support_level": null,
          "aa_start": 979,
          "aa_end": null,
          "aa_length": 1272,
          "cds_start": 2935,
          "cds_end": null,
          "cds_length": 3819,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000698836.1"
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLEKHA7",
          "gene_hgnc_id": 27049,
          "hgvs_c": "c.2935A>C",
          "hgvs_p": "p.Arg979Arg",
          "transcript": "ENST00000917925.1",
          "protein_id": "ENSP00000587984.1",
          "transcript_support_level": null,
          "aa_start": 979,
          "aa_end": null,
          "aa_length": 1219,
          "cds_start": 2935,
          "cds_end": null,
          "cds_length": 3660,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000917925.1"
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLEKHA7",
          "gene_hgnc_id": 27049,
          "hgvs_c": "c.2563A>C",
          "hgvs_p": "p.Arg855Arg",
          "transcript": "ENST00000637162.1",
          "protein_id": "ENSP00000489780.1",
          "transcript_support_level": 5,
          "aa_start": 855,
          "aa_end": null,
          "aa_length": 1191,
          "cds_start": 2563,
          "cds_end": null,
          "cds_length": 3576,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000637162.1"
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLEKHA7",
          "gene_hgnc_id": 27049,
          "hgvs_c": "c.2935A>C",
          "hgvs_p": "p.Arg979Arg",
          "transcript": "NM_001329631.2",
          "protein_id": "NP_001316560.1",
          "transcript_support_level": null,
          "aa_start": 979,
          "aa_end": null,
          "aa_length": 1122,
          "cds_start": 2935,
          "cds_end": null,
          "cds_length": 3369,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001329631.2"
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLEKHA7",
          "gene_hgnc_id": 27049,
          "hgvs_c": "c.2932A>C",
          "hgvs_p": "p.Arg978Arg",
          "transcript": "NM_175058.5",
          "protein_id": "NP_778228.3",
          "transcript_support_level": null,
          "aa_start": 978,
          "aa_end": null,
          "aa_length": 1121,
          "cds_start": 2932,
          "cds_end": null,
          "cds_length": 3366,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_175058.5"
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLEKHA7",
          "gene_hgnc_id": 27049,
          "hgvs_c": "c.2803A>C",
          "hgvs_p": "p.Arg935Arg",
          "transcript": "ENST00000696749.1",
          "protein_id": "ENSP00000512848.1",
          "transcript_support_level": null,
          "aa_start": 935,
          "aa_end": null,
          "aa_length": 1078,
          "cds_start": 2803,
          "cds_end": null,
          "cds_length": 3237,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000696749.1"
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLEKHA7",
          "gene_hgnc_id": 27049,
          "hgvs_c": "c.1150A>C",
          "hgvs_p": "p.Arg384Arg",
          "transcript": "ENST00000636113.1",
          "protein_id": "ENSP00000490177.1",
          "transcript_support_level": 5,
          "aa_start": 384,
          "aa_end": null,
          "aa_length": 527,
          "cds_start": 1150,
          "cds_end": null,
          "cds_length": 1584,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000636113.1"
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLEKHA7",
          "gene_hgnc_id": 27049,
          "hgvs_c": "c.595A>C",
          "hgvs_p": "p.Arg199Arg",
          "transcript": "ENST00000636090.1",
          "protein_id": "ENSP00000490167.1",
          "transcript_support_level": 5,
          "aa_start": 199,
          "aa_end": null,
          "aa_length": 518,
          "cds_start": 595,
          "cds_end": null,
          "cds_length": 1557,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000636090.1"
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 22,
          "exon_rank_end": null,
          "exon_count": 29,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLEKHA7",
          "gene_hgnc_id": 27049,
          "hgvs_c": "c.3136A>C",
          "hgvs_p": "p.Arg1046Arg",
          "transcript": "XM_047426426.1",
          "protein_id": "XP_047282382.1",
          "transcript_support_level": null,
          "aa_start": 1046,
          "aa_end": null,
          "aa_length": 1365,
          "cds_start": 3136,
          "cds_end": null,
          "cds_length": 4098,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "XM_047426426.1"
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 22,
          "exon_rank_end": null,
          "exon_count": 29,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLEKHA7",
          "gene_hgnc_id": 27049,
          "hgvs_c": "c.3133A>C",
          "hgvs_p": "p.Arg1045Arg",
          "transcript": "XM_024448357.2",
          "protein_id": "XP_024304125.1",
          "transcript_support_level": null,
          "aa_start": 1045,
          "aa_end": null,
          "aa_length": 1364,
          "cds_start": 3133,
          "cds_end": null,
          "cds_length": 4095,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "XM_024448357.2"
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 22,
          "exon_rank_end": null,
          "exon_count": 29,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLEKHA7",
          "gene_hgnc_id": 27049,
          "hgvs_c": "c.3136A>C",
          "hgvs_p": "p.Arg1046Arg",
          "transcript": "XM_024448358.2",
          "protein_id": "XP_024304126.1",
          "transcript_support_level": null,
          "aa_start": 1046,
          "aa_end": null,
          "aa_length": 1339,
          "cds_start": 3136,
          "cds_end": null,
          "cds_length": 4020,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "XM_024448358.2"
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLEKHA7",
          "gene_hgnc_id": 27049,
          "hgvs_c": "c.3055A>C",
          "hgvs_p": "p.Arg1019Arg",
          "transcript": "XM_047426427.1",
          "protein_id": "XP_047282383.1",
          "transcript_support_level": null,
          "aa_start": 1019,
          "aa_end": null,
          "aa_length": 1338,
          "cds_start": 3055,
          "cds_end": null,
          "cds_length": 4017,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "XM_047426427.1"
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLEKHA7",
          "gene_hgnc_id": 27049,
          "hgvs_c": "c.3016A>C",
          "hgvs_p": "p.Arg1006Arg",
          "transcript": "XM_047426428.1",
          "protein_id": "XP_047282384.1",
          "transcript_support_level": null,
          "aa_start": 1006,
          "aa_end": null,
          "aa_length": 1325,
          "cds_start": 3016,
          "cds_end": null,
          "cds_length": 3978,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "XM_047426428.1"
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
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          "verdict": "Likely_benign",
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      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
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  "message": null
}