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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: 17-19672408-A-G (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=17&pos=19672408&ref=A&alt=G&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "17",
      "pos": 19672408,
      "ref": "A",
      "alt": "G",
      "effect": "intron_variant",
      "transcript": "NM_001031806.2",
      "consequences": [
        {
          "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": 10,
          "intron_rank": 9,
          "intron_rank_end": null,
          "gene_symbol": "ALDH3A2",
          "gene_hgnc_id": 403,
          "hgvs_c": "c.1443+452A>G",
          "hgvs_p": null,
          "transcript": "NM_000382.3",
          "protein_id": "NP_000373.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 485,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1458,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000176643.11",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_000382.3"
        },
        {
          "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": 10,
          "intron_rank": 9,
          "intron_rank_end": null,
          "gene_symbol": "ALDH3A2",
          "gene_hgnc_id": 403,
          "hgvs_c": "c.1443+452A>G",
          "hgvs_p": null,
          "transcript": "ENST00000176643.11",
          "protein_id": "ENSP00000176643.6",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 485,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1458,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_000382.3",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000176643.11"
        },
        {
          "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": 11,
          "intron_rank": 9,
          "intron_rank_end": null,
          "gene_symbol": "ALDH3A2",
          "gene_hgnc_id": 403,
          "hgvs_c": "c.1443+452A>G",
          "hgvs_p": null,
          "transcript": "ENST00000339618.8",
          "protein_id": "ENSP00000345774.4",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 508,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1527,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000339618.8"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": 6,
          "intron_rank_end": null,
          "gene_symbol": "ALDH3A2",
          "gene_hgnc_id": 403,
          "hgvs_c": "n.1193+452A>G",
          "hgvs_p": null,
          "transcript": "ENST00000476965.5",
          "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": "retained_intron",
          "feature": "ENST00000476965.5"
        },
        {
          "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": 10,
          "intron_rank": 9,
          "intron_rank_end": null,
          "gene_symbol": "ALDH3A2",
          "gene_hgnc_id": 403,
          "hgvs_c": "c.1443+452A>G",
          "hgvs_p": null,
          "transcript": "ENST00000671878.1",
          "protein_id": "ENSP00000500516.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 521,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1566,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000671878.1"
        },
        {
          "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": 11,
          "intron_rank": 10,
          "intron_rank_end": null,
          "gene_symbol": "ALDH3A2",
          "gene_hgnc_id": 403,
          "hgvs_c": "c.1443+452A>G",
          "hgvs_p": null,
          "transcript": "ENST00000672465.1",
          "protein_id": "ENSP00000500517.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 521,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1566,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000672465.1"
        },
        {
          "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": 11,
          "intron_rank": 9,
          "intron_rank_end": null,
          "gene_symbol": "ALDH3A2",
          "gene_hgnc_id": 403,
          "hgvs_c": "c.1443+452A>G",
          "hgvs_p": null,
          "transcript": "NM_001031806.2",
          "protein_id": "NP_001026976.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 508,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1527,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001031806.2"
        },
        {
          "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": 12,
          "intron_rank": 10,
          "intron_rank_end": null,
          "gene_symbol": "ALDH3A2",
          "gene_hgnc_id": 403,
          "hgvs_c": "c.1443+452A>G",
          "hgvs_p": null,
          "transcript": "NM_001369136.1",
          "protein_id": "NP_001356065.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 508,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1527,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001369136.1"
        },
        {
          "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": 12,
          "intron_rank": 10,
          "intron_rank_end": null,
          "gene_symbol": "ALDH3A2",
          "gene_hgnc_id": 403,
          "hgvs_c": "c.1443+452A>G",
          "hgvs_p": null,
          "transcript": "NM_001369137.2",
          "protein_id": "NP_001356066.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 508,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1527,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001369137.2"
        },
        {
          "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": 11,
          "intron_rank": 10,
          "intron_rank_end": null,
          "gene_symbol": "ALDH3A2",
          "gene_hgnc_id": 403,
          "hgvs_c": "c.1443+452A>G",
          "hgvs_p": null,
          "transcript": "NM_001369138.2",
          "protein_id": "NP_001356067.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 485,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1458,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001369138.2"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 11,
          "intron_rank": 10,
          "intron_rank_end": null,
          "gene_symbol": "ALDH3A2",
          "gene_hgnc_id": 403,
          "hgvs_c": "c.1443+452A>G",
          "hgvs_p": null,
          "transcript": "NM_001369139.1",
          "protein_id": "NP_001356068.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 485,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1458,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001369139.1"
        },
        {
          "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": 11,
          "intron_rank": 10,
          "intron_rank_end": null,
          "gene_symbol": "ALDH3A2",
          "gene_hgnc_id": 403,
          "hgvs_c": "c.1443+452A>G",
          "hgvs_p": null,
          "transcript": "ENST00000579855.5",
          "protein_id": "ENSP00000463637.1",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 485,
          "cds_start": null,
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          "cdna_start": null,
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          "cdna_length": null,
          "mane_select": null,
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          "biotype": "protein_coding",
          "feature": "ENST00000579855.5"
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
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          "intron_rank": 10,
          "intron_rank_end": null,
          "gene_symbol": "ALDH3A2",
          "gene_hgnc_id": 403,
          "hgvs_c": "c.1443+452A>G",
          "hgvs_p": null,
          "transcript": "ENST00000581518.6",
          "protein_id": "ENSP00000461916.2",
          "transcript_support_level": 5,
          "aa_start": null,
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          "aa_length": 485,
          "cds_start": null,
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          "cdna_start": null,
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        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
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          ],
          "exon_rank": null,
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          "exon_count": 11,
          "intron_rank": 10,
          "intron_rank_end": null,
          "gene_symbol": "ALDH3A2",
          "gene_hgnc_id": 403,
          "hgvs_c": "c.1443+452A>G",
          "hgvs_p": null,
          "transcript": "ENST00000672357.1",
          "protein_id": "ENSP00000500092.1",
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          "aa_start": null,
          "aa_end": null,
          "aa_length": 485,
          "cds_start": null,
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        },
        {
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          ],
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          "gene_symbol": "ALDH3A2",
          "gene_hgnc_id": 403,
          "hgvs_c": "c.1443+452A>G",
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          "transcript": "ENST00000877756.1",
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          "biotype": "protein_coding",
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        },
        {
          "aa_ref": null,
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          "canonical": false,
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          "strand": true,
          "consequences": [
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          ],
          "exon_rank": null,
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          "exon_count": 11,
          "intron_rank": 10,
          "intron_rank_end": null,
          "gene_symbol": "ALDH3A2",
          "gene_hgnc_id": 403,
          "hgvs_c": "c.1443+452A>G",
          "hgvs_p": null,
          "transcript": "ENST00000877757.1",
          "protein_id": "ENSP00000547816.1",
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          "feature": "ENST00000877757.1"
        },
        {
          "aa_ref": null,
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          ],
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          "exon_count": 10,
          "intron_rank": 9,
          "intron_rank_end": null,
          "gene_symbol": "ALDH3A2",
          "gene_hgnc_id": 403,
          "hgvs_c": "c.1447+448A>G",
          "hgvs_p": null,
          "transcript": "ENST00000948947.1",
          "protein_id": "ENSP00000619006.1",
          "transcript_support_level": null,
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        {
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          "gene_symbol": "ALDH3A2",
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          "transcript": "ENST00000877753.1",
          "protein_id": "ENSP00000547812.1",
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        },
        {
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          ],
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          "hgvs_c": "c.1410+452A>G",
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          "transcript": "ENST00000932536.1",
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          "biotype": "protein_coding",
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        },
        {
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": 9,
          "intron_rank_end": null,
          "gene_symbol": "ALDH3A2",
          "gene_hgnc_id": 403,
          "hgvs_c": "c.1296+452A>G",
          "hgvs_p": null,
          "transcript": "ENST00000672709.1",
          "protein_id": "ENSP00000499877.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 459,
          "cds_start": null,
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          "cds_length": 1380,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
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          "biotype": "protein_coding",
          "feature": "ENST00000672709.1"
        },
        {
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          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
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      "acmg_classification": "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
}