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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: 4-109433885-G-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=4&pos=109433885&ref=G&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "4",
      "pos": 109433885,
      "ref": "G",
      "alt": "C",
      "effect": "missense_variant",
      "transcript": "NM_001300813.3",
      "consequences": [
        {
          "aa_ref": "G",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SEC24B",
          "gene_hgnc_id": 10704,
          "hgvs_c": "c.16G>C",
          "hgvs_p": "p.Gly6Arg",
          "transcript": "NM_006323.5",
          "protein_id": "NP_006314.2",
          "transcript_support_level": null,
          "aa_start": 6,
          "aa_end": null,
          "aa_length": 1268,
          "cds_start": 16,
          "cds_end": null,
          "cds_length": 3807,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000265175.5",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_006323.5"
        },
        {
          "aa_ref": "G",
          "aa_alt": "R",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SEC24B",
          "gene_hgnc_id": 10704,
          "hgvs_c": "c.16G>C",
          "hgvs_p": "p.Gly6Arg",
          "transcript": "ENST00000265175.5",
          "protein_id": "ENSP00000265175.4",
          "transcript_support_level": 1,
          "aa_start": 6,
          "aa_end": null,
          "aa_length": 1268,
          "cds_start": 16,
          "cds_end": null,
          "cds_length": 3807,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_006323.5",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000265175.5"
        },
        {
          "aa_ref": "G",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SEC24B",
          "gene_hgnc_id": 10704,
          "hgvs_c": "c.16G>C",
          "hgvs_p": "p.Gly6Arg",
          "transcript": "ENST00000504968.6",
          "protein_id": "ENSP00000428564.1",
          "transcript_support_level": 1,
          "aa_start": 6,
          "aa_end": null,
          "aa_length": 1298,
          "cds_start": 16,
          "cds_end": null,
          "cds_length": 3897,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000504968.6"
        },
        {
          "aa_ref": "G",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SEC24B",
          "gene_hgnc_id": 10704,
          "hgvs_c": "c.16G>C",
          "hgvs_p": "p.Gly6Arg",
          "transcript": "ENST00000399100.6",
          "protein_id": "ENSP00000382051.2",
          "transcript_support_level": 1,
          "aa_start": 6,
          "aa_end": null,
          "aa_length": 1233,
          "cds_start": 16,
          "cds_end": null,
          "cds_length": 3702,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000399100.6"
        },
        {
          "aa_ref": "G",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SEC24B",
          "gene_hgnc_id": 10704,
          "hgvs_c": "c.16G>C",
          "hgvs_p": "p.Gly6Arg",
          "transcript": "ENST00000898583.1",
          "protein_id": "ENSP00000568642.1",
          "transcript_support_level": null,
          "aa_start": 6,
          "aa_end": null,
          "aa_length": 1299,
          "cds_start": 16,
          "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": "ENST00000898583.1"
        },
        {
          "aa_ref": "G",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SEC24B",
          "gene_hgnc_id": 10704,
          "hgvs_c": "c.16G>C",
          "hgvs_p": "p.Gly6Arg",
          "transcript": "NM_001300813.3",
          "protein_id": "NP_001287742.1",
          "transcript_support_level": null,
          "aa_start": 6,
          "aa_end": null,
          "aa_length": 1298,
          "cds_start": 16,
          "cds_end": null,
          "cds_length": 3897,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001300813.3"
        },
        {
          "aa_ref": "G",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SEC24B",
          "gene_hgnc_id": 10704,
          "hgvs_c": "c.16G>C",
          "hgvs_p": "p.Gly6Arg",
          "transcript": "ENST00000934097.1",
          "protein_id": "ENSP00000604156.1",
          "transcript_support_level": null,
          "aa_start": 6,
          "aa_end": null,
          "aa_length": 1284,
          "cds_start": 16,
          "cds_end": null,
          "cds_length": 3855,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000934097.1"
        },
        {
          "aa_ref": "G",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SEC24B",
          "gene_hgnc_id": 10704,
          "hgvs_c": "c.16G>C",
          "hgvs_p": "p.Gly6Arg",
          "transcript": "ENST00000898588.1",
          "protein_id": "ENSP00000568647.1",
          "transcript_support_level": null,
          "aa_start": 6,
          "aa_end": null,
          "aa_length": 1272,
          "cds_start": 16,
          "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": "ENST00000898588.1"
        },
        {
          "aa_ref": "G",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SEC24B",
          "gene_hgnc_id": 10704,
          "hgvs_c": "c.16G>C",
          "hgvs_p": "p.Gly6Arg",
          "transcript": "NM_001318085.2",
          "protein_id": "NP_001305014.1",
          "transcript_support_level": null,
          "aa_start": 6,
          "aa_end": null,
          "aa_length": 1267,
          "cds_start": 16,
          "cds_end": null,
          "cds_length": 3804,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001318085.2"
        },
        {
          "aa_ref": "G",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SEC24B",
          "gene_hgnc_id": 10704,
          "hgvs_c": "c.16G>C",
          "hgvs_p": "p.Gly6Arg",
          "transcript": "ENST00000898581.1",
          "protein_id": "ENSP00000568640.1",
          "transcript_support_level": null,
          "aa_start": 6,
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          "aa_length": 1267,
          "cds_start": 16,
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          "cdna_start": null,
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          "mane_select": null,
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          "biotype": "protein_coding",
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        },
        {
          "aa_ref": "G",
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          "consequences": [
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          ],
          "exon_rank": 1,
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          "exon_count": 24,
          "intron_rank": null,
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          "gene_symbol": "SEC24B",
          "gene_hgnc_id": 10704,
          "hgvs_c": "c.16G>C",
          "hgvs_p": "p.Gly6Arg",
          "transcript": "ENST00000950647.1",
          "protein_id": "ENSP00000620706.1",
          "transcript_support_level": null,
          "aa_start": 6,
          "aa_end": null,
          "aa_length": 1265,
          "cds_start": 16,
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          "cds_length": 3798,
          "cdna_start": null,
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          "mane_select": null,
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          "biotype": "protein_coding",
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        },
        {
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          "canonical": false,
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          "strand": true,
          "consequences": [
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          "exon_count": 24,
          "intron_rank": null,
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          "gene_symbol": "SEC24B",
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          "hgvs_c": "c.16G>C",
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          "transcript": "ENST00000898587.1",
          "protein_id": "ENSP00000568646.1",
          "transcript_support_level": null,
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          "cds_start": 16,
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          "cdna_start": null,
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          "mane_select": null,
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        },
        {
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          ],
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          "gene_symbol": "SEC24B",
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          "hgvs_c": "c.16G>C",
          "hgvs_p": "p.Gly6Arg",
          "transcript": "ENST00000898586.1",
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        {
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          ],
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          "intron_rank": null,
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          "gene_symbol": "SEC24B",
          "gene_hgnc_id": 10704,
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          "hgvs_p": "p.Gly6Arg",
          "transcript": "ENST00000934099.1",
          "protein_id": "ENSP00000604158.1",
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        {
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        {
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          ],
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          "gene_symbol": "SEC24B",
          "gene_hgnc_id": 10704,
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          "hgvs_p": "p.Gly6Arg",
          "transcript": "ENST00000950644.1",
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        {
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          "intron_rank": null,
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          "gene_symbol": "SEC24B",
          "gene_hgnc_id": 10704,
          "hgvs_c": "c.16G>C",
          "hgvs_p": "p.Gly6Arg",
          "transcript": "NM_001042734.4",
          "protein_id": "NP_001036199.1",
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        {
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          "gene_symbol": "SEC24B",
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        {
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        },
        {
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          ],
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          "intron_rank": null,
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          "gene_symbol": "SEC24B",
          "gene_hgnc_id": 10704,
          "hgvs_c": "c.16G>C",
          "hgvs_p": "p.Gly6Arg",
          "transcript": "ENST00000898591.1",
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          "transcript_support_level": null,
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          "biotype": "protein_coding",
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        },
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      "splice_source_selected": "max_spliceai",
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      "bayesdelnoaf_prediction": "Uncertain_significance",
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      "acmg_classification": "Uncertain_significance",
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          "verdict": "Uncertain_significance",
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        {
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          "verdict": "Uncertain_significance",
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          "effects": [
            "intron_variant"
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          "inheritance_mode": "",
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      ],
      "clinvar_disease": "not specified",
      "clinvar_classification": "Uncertain significance",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "US:1",
      "phenotype_combined": "not specified",
      "pathogenicity_classification_combined": "Uncertain significance",
      "custom_annotations": null
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  ],
  "message": null
}