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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: 1-16562549-T-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=1&pos=16562549&ref=T&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "1",
      "pos": 16562549,
      "ref": "T",
      "alt": "A",
      "effect": "3_prime_UTR_variant",
      "transcript": "ENST00000430580.6",
      "consequences": [
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 27,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NBPF1",
          "gene_hgnc_id": 26088,
          "hgvs_c": "c.*1394A>T",
          "hgvs_p": null,
          "transcript": "NM_001405666.3",
          "protein_id": "NP_001392595.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1087,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3264,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5935,
          "mane_select": "ENST00000713538.1",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 29,
          "exon_rank_end": null,
          "exon_count": 29,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NBPF1",
          "gene_hgnc_id": 26088,
          "hgvs_c": "c.*1394A>T",
          "hgvs_p": null,
          "transcript": "ENST00000430580.6",
          "protein_id": "ENSP00000474456.1",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1139,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3420,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5932,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 29,
          "exon_rank_end": null,
          "exon_count": 29,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NBPF1",
          "gene_hgnc_id": 26088,
          "hgvs_c": "c.*1394A>T",
          "hgvs_p": null,
          "transcript": "NM_001405667.2",
          "protein_id": "NP_001392596.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1153,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3462,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 6137,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 29,
          "exon_rank_end": null,
          "exon_count": 29,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NBPF1",
          "gene_hgnc_id": 26088,
          "hgvs_c": "c.*1394A>T",
          "hgvs_p": null,
          "transcript": "NM_001405680.2",
          "protein_id": "NP_001392609.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1150,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3453,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5942,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 29,
          "exon_rank_end": null,
          "exon_count": 29,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NBPF1",
          "gene_hgnc_id": 26088,
          "hgvs_c": "c.*1394A>T",
          "hgvs_p": null,
          "transcript": "NM_001405681.2",
          "protein_id": "NP_001392610.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1150,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3453,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 6128,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 30,
          "exon_rank_end": null,
          "exon_count": 30,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NBPF1",
          "gene_hgnc_id": 26088,
          "hgvs_c": "c.*1394A>T",
          "hgvs_p": null,
          "transcript": "NM_001405682.2",
          "protein_id": "NP_001392611.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1150,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3453,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5972,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 28,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NBPF1",
          "gene_hgnc_id": 26088,
          "hgvs_c": "c.*1394A>T",
          "hgvs_p": null,
          "transcript": "NM_001405668.2",
          "protein_id": "NP_001392597.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1125,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3378,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5867,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 28,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NBPF1",
          "gene_hgnc_id": 26088,
          "hgvs_c": "c.*1394A>T",
          "hgvs_p": null,
          "transcript": "NM_001405669.2",
          "protein_id": "NP_001392598.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1125,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3378,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5770,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 29,
          "exon_rank_end": null,
          "exon_count": 29,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NBPF1",
          "gene_hgnc_id": 26088,
          "hgvs_c": "c.*1394A>T",
          "hgvs_p": null,
          "transcript": "NM_001405670.2",
          "protein_id": "NP_001392599.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 1125,
          "cds_start": -4,
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          "cdna_start": null,
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          "cdna_length": 5893,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 28,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NBPF1",
          "gene_hgnc_id": 26088,
          "hgvs_c": "c.*1394A>T",
          "hgvs_p": null,
          "transcript": "NM_001405671.2",
          "protein_id": "NP_001392600.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 1125,
          "cds_start": -4,
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          "cdna_start": null,
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          "cdna_length": 6049,
          "mane_select": null,
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        {
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          "canonical": false,
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          "exon_rank_end": null,
          "exon_count": 29,
          "intron_rank": null,
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          "gene_symbol": "NBPF1",
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          "hgvs_c": "c.*1394A>T",
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          "protein_id": "NP_001392601.1",
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          "cdna_start": null,
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          "mane_select": null,
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        {
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          "canonical": false,
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          "strand": false,
          "consequences": [
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          "exon_count": 28,
          "intron_rank": null,
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          "gene_symbol": "NBPF1",
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          "hgvs_c": "c.*1394A>T",
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          "exon_count": 29,
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          "gene_symbol": "NBPF1",
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          "intron_rank": null,
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          "gene_symbol": "NBPF1",
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        {
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          "gene_symbol": "NBPF1",
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          "intron_rank": null,
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          "gene_symbol": "NBPF1",
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        {
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          "gene_symbol": "NBPF1",
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        {
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          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": null,
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          "gene_symbol": "NBPF1",
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          "hgvs_c": "c.*1394A>T",
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      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
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      "custom_annotations": null
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  "message": null
}