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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: 6-104744232-T-TAAC (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=6&pos=104744232&ref=T&alt=TAAC&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "6",
      "pos": 104744232,
      "ref": "T",
      "alt": "TAAC",
      "effect": "splice_region_variant,intron_variant",
      "transcript": "NM_020771.4",
      "consequences": [
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": 21,
          "intron_rank_end": null,
          "gene_symbol": "HACE1",
          "gene_hgnc_id": 21033,
          "hgvs_c": "c.2443-5_2443-3dupGTT",
          "hgvs_p": null,
          "transcript": "NM_020771.4",
          "protein_id": "NP_065822.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 909,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2730,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000262903.9",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_020771.4"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": 21,
          "intron_rank_end": null,
          "gene_symbol": "HACE1",
          "gene_hgnc_id": 21033,
          "hgvs_c": "c.2443-3_2443-2insGTT",
          "hgvs_p": null,
          "transcript": "ENST00000262903.9",
          "protein_id": "ENSP00000262903.4",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 909,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2730,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_020771.4",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000262903.9"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": 10,
          "intron_rank_end": null,
          "gene_symbol": "HACE1",
          "gene_hgnc_id": 21033,
          "hgvs_c": "n.3464-3_3464-2insGTT",
          "hgvs_p": null,
          "transcript": "ENST00000369127.8",
          "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": "retained_intron",
          "feature": "ENST00000369127.8"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": 23,
          "intron_rank_end": null,
          "gene_symbol": "HACE1",
          "gene_hgnc_id": 21033,
          "hgvs_c": "n.*2105-3_*2105-2insGTT",
          "hgvs_p": null,
          "transcript": "ENST00000416605.6",
          "protein_id": "ENSP00000392425.2",
          "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": "nonsense_mediated_decay",
          "feature": "ENST00000416605.6"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "HACE1",
          "gene_hgnc_id": 21033,
          "hgvs_c": "n.957-3_957-2insGTT",
          "hgvs_p": null,
          "transcript": "ENST00000517995.5",
          "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": "pseudogene",
          "feature": "ENST00000517995.5"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": 21,
          "intron_rank_end": null,
          "gene_symbol": "HACE1",
          "gene_hgnc_id": 21033,
          "hgvs_c": "c.2476-3_2476-2insGTT",
          "hgvs_p": null,
          "transcript": "ENST00000851410.1",
          "protein_id": "ENSP00000521469.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 920,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2763,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000851410.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": 21,
          "intron_rank_end": null,
          "gene_symbol": "HACE1",
          "gene_hgnc_id": 21033,
          "hgvs_c": "c.2443-3_2443-2insGTT",
          "hgvs_p": null,
          "transcript": "ENST00000851409.1",
          "protein_id": "ENSP00000521468.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 907,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2724,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000851409.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": 21,
          "intron_rank_end": null,
          "gene_symbol": "HACE1",
          "gene_hgnc_id": 21033,
          "hgvs_c": "c.2368-3_2368-2insGTT",
          "hgvs_p": null,
          "transcript": "ENST00000950221.1",
          "protein_id": "ENSP00000620280.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 884,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2655,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000950221.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": 20,
          "intron_rank_end": null,
          "gene_symbol": "HACE1",
          "gene_hgnc_id": 21033,
          "hgvs_c": "c.2353-3_2353-2insGTT",
          "hgvs_p": null,
          "transcript": "ENST00000914227.1",
          "protein_id": "ENSP00000584286.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 879,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2640,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000914227.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": 20,
          "intron_rank_end": null,
          "gene_symbol": "HACE1",
          "gene_hgnc_id": 21033,
          "hgvs_c": "c.2353-3_2353-2insGTT",
          "hgvs_p": null,
          "transcript": "ENST00000950219.1",
          "protein_id": "ENSP00000620278.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 877,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2634,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000950219.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": 20,
          "intron_rank_end": null,
          "gene_symbol": "HACE1",
          "gene_hgnc_id": 21033,
          "hgvs_c": "c.2344-3_2344-2insGTT",
          "hgvs_p": null,
          "transcript": "ENST00000914226.1",
          "protein_id": "ENSP00000584285.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 876,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2631,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000914226.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": 21,
          "intron_rank_end": null,
          "gene_symbol": "HACE1",
          "gene_hgnc_id": 21033,
          "hgvs_c": "c.2341-5_2341-3dupGTT",
          "hgvs_p": null,
          "transcript": "NM_001321083.2",
          "protein_id": "NP_001308012.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 875,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2628,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001321083.2"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": 21,
          "intron_rank_end": null,
          "gene_symbol": "HACE1",
          "gene_hgnc_id": 21033,
          "hgvs_c": "c.2443-3_2443-2insGTT",
          "hgvs_p": null,
          "transcript": "ENST00000950220.1",
          "protein_id": "ENSP00000620279.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 871,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2616,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000950220.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": 20,
          "intron_rank_end": null,
          "gene_symbol": "HACE1",
          "gene_hgnc_id": 21033,
          "hgvs_c": "c.2311-5_2311-3dupGTT",
          "hgvs_p": null,
          "transcript": "NM_001321080.2",
          "protein_id": "NP_001308009.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 865,
          "cds_start": null,
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          "cds_length": 2598,
          "cdna_start": null,
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          "cdna_length": null,
          "mane_select": null,
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          "biotype": "protein_coding",
          "feature": "NM_001321080.2"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": 19,
          "intron_rank_end": null,
          "gene_symbol": "HACE1",
          "gene_hgnc_id": 21033,
          "hgvs_c": "c.2221-3_2221-2insGTT",
          "hgvs_p": null,
          "transcript": "ENST00000851408.1",
          "protein_id": "ENSP00000521467.1",
          "transcript_support_level": null,
          "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": "ENST00000851408.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": 21,
          "intron_rank_end": null,
          "gene_symbol": "HACE1",
          "gene_hgnc_id": 21033,
          "hgvs_c": "c.2209-5_2209-3dupGTT",
          "hgvs_p": null,
          "transcript": "NM_001350554.2",
          "protein_id": "NP_001337483.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 831,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2496,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001350554.2"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": 18,
          "intron_rank_end": null,
          "gene_symbol": "HACE1",
          "gene_hgnc_id": 21033,
          "hgvs_c": "c.2152-5_2152-3dupGTT",
          "hgvs_p": null,
          "transcript": "NM_001350555.2",
          "protein_id": "NP_001337484.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 812,
          "cds_start": null,
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          "cds_length": 2439,
          "cdna_start": null,
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          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001350555.2"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": 18,
          "intron_rank_end": null,
          "gene_symbol": "HACE1",
          "gene_hgnc_id": 21033,
          "hgvs_c": "c.2152-3_2152-2insGTT",
          "hgvs_p": null,
          "transcript": "ENST00000851407.1",
          "protein_id": "ENSP00000521466.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 812,
          "cds_start": null,
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          "cds_length": 2439,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000851407.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": 17,
          "intron_rank_end": null,
          "gene_symbol": "HACE1",
          "gene_hgnc_id": 21033,
          "hgvs_c": "c.2047-3_2047-2insGTT",
          "hgvs_p": null,
          "transcript": "ENST00000950222.1",
          "protein_id": "ENSP00000620281.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 777,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2334,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000950222.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": 20,
          "intron_rank_end": null,
          "gene_symbol": "HACE1",
          "gene_hgnc_id": 21033,
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          "verdict": "Uncertain_significance",
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      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
    }
  ],
  "message": null
}