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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: 4-105700486-T-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=4&pos=105700486&ref=T&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "4",
      "pos": 105700486,
      "ref": "T",
      "alt": "C",
      "effect": "intron_variant",
      "transcript": "NM_020395.4",
      "consequences": [
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "INTS12",
          "gene_hgnc_id": 25067,
          "hgvs_c": "c.-9-472A>G",
          "hgvs_p": null,
          "transcript": "NM_020395.4",
          "protein_id": "NP_065128.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 462,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1389,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1718,
          "mane_select": "ENST00000340139.10",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_020395.4"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "INTS12",
          "gene_hgnc_id": 25067,
          "hgvs_c": "c.-9-472A>G",
          "hgvs_p": null,
          "transcript": "ENST00000340139.10",
          "protein_id": "ENSP00000340737.5",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 462,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1389,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1718,
          "mane_select": "NM_020395.4",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000340139.10"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "INTS12",
          "gene_hgnc_id": 25067,
          "hgvs_c": "c.-9-472A>G",
          "hgvs_p": null,
          "transcript": "ENST00000451321.6",
          "protein_id": "ENSP00000415433.2",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 462,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1389,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1975,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000451321.6"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "5_prime_UTR_premature_start_codon_gain_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "INTS12",
          "gene_hgnc_id": 25067,
          "hgvs_c": "c.-481A>G",
          "hgvs_p": null,
          "transcript": "ENST00000891062.1",
          "protein_id": "ENSP00000561121.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 462,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1389,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2508,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000891062.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "5_prime_UTR_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "INTS12",
          "gene_hgnc_id": 25067,
          "hgvs_c": "c.-481A>G",
          "hgvs_p": null,
          "transcript": "ENST00000891062.1",
          "protein_id": "ENSP00000561121.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 462,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1389,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2508,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000891062.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "INTS12",
          "gene_hgnc_id": 25067,
          "hgvs_c": "c.-9-472A>G",
          "hgvs_p": null,
          "transcript": "NM_001142471.2",
          "protein_id": "NP_001135943.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 462,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1389,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1556,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001142471.2"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "INTS12",
          "gene_hgnc_id": 25067,
          "hgvs_c": "c.-9-472A>G",
          "hgvs_p": null,
          "transcript": "ENST00000394735.5",
          "protein_id": "ENSP00000378221.1",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 462,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1389,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1927,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000394735.5"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "INTS12",
          "gene_hgnc_id": 25067,
          "hgvs_c": "c.-9-472A>G",
          "hgvs_p": null,
          "transcript": "ENST00000891042.1",
          "protein_id": "ENSP00000561101.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 462,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1389,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2341,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000891042.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 8,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "INTS12",
          "gene_hgnc_id": 25067,
          "hgvs_c": "c.-9-472A>G",
          "hgvs_p": null,
          "transcript": "ENST00000891043.1",
          "protein_id": "ENSP00000561102.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 462,
          "cds_start": null,
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          "cds_length": 1389,
          "cdna_start": null,
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          "cdna_length": 3024,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000891043.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "INTS12",
          "gene_hgnc_id": 25067,
          "hgvs_c": "c.-9-472A>G",
          "hgvs_p": null,
          "transcript": "ENST00000891046.1",
          "protein_id": "ENSP00000561105.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 462,
          "cds_start": null,
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          "cdna_start": null,
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          "mane_select": null,
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        {
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          "consequences": [
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          "intron_rank": 3,
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          "gene_symbol": "INTS12",
          "gene_hgnc_id": 25067,
          "hgvs_c": "c.-9-472A>G",
          "hgvs_p": null,
          "transcript": "ENST00000891048.1",
          "protein_id": "ENSP00000561107.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 462,
          "cds_start": null,
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          "cdna_start": null,
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          "mane_select": null,
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        {
          "aa_ref": null,
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          "canonical": false,
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          "gene_symbol": "INTS12",
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        {
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          "gene_symbol": "INTS12",
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          "hgvs_c": "c.-9-472A>G",
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          "transcript": "ENST00000891053.1",
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        {
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          "gene_symbol": "INTS12",
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          "gene_symbol": "INTS12",
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          "transcript": "ENST00000891056.1",
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          "gene_symbol": "INTS12",
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          "transcript": "ENST00000891059.1",
          "protein_id": "ENSP00000561118.1",
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          "consequences": [
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}
For research and educational, non-commercial use only. Not for clinical or diagnostic use. GeneBe does not provide medical advice. Data use for AI modeling is prohibited: if used, the cost is $0.001 per byte of downloaded uncompressed data.