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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: 15-40303426-G-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=15&pos=40303426&ref=G&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "15",
      "pos": 40303426,
      "ref": "G",
      "alt": "C",
      "effect": "intron_variant",
      "transcript": "ENST00000260402.8",
      "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": 32,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "PLCB2",
          "gene_hgnc_id": 9055,
          "hgvs_c": "c.163-70C>G",
          "hgvs_p": null,
          "transcript": "NM_004573.3",
          "protein_id": "NP_004564.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1185,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3558,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4627,
          "mane_select": "ENST00000260402.8",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "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": 32,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "PLCB2",
          "gene_hgnc_id": 9055,
          "hgvs_c": "c.163-70C>G",
          "hgvs_p": null,
          "transcript": "ENST00000260402.8",
          "protein_id": "ENSP00000260402.3",
          "transcript_support_level": 2,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1185,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3558,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4627,
          "mane_select": "NM_004573.3",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "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": 32,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "PLCB2",
          "gene_hgnc_id": 9055,
          "hgvs_c": "c.163-70C>G",
          "hgvs_p": null,
          "transcript": "ENST00000557821.5",
          "protein_id": "ENSP00000453975.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1181,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3546,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4517,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "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": 31,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "PLCB2",
          "gene_hgnc_id": 9055,
          "hgvs_c": "c.163-70C>G",
          "hgvs_p": null,
          "transcript": "ENST00000456256.6",
          "protein_id": "ENSP00000411991.2",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1170,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3513,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4242,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "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": "PLCB2",
          "gene_hgnc_id": 9055,
          "hgvs_c": "c.163-70C>G",
          "hgvs_p": null,
          "transcript": "ENST00000543785.3",
          "protein_id": "ENSP00000444652.2",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 199,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 600,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1763,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "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": 32,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "PLCB2",
          "gene_hgnc_id": 9055,
          "hgvs_c": "c.163-70C>G",
          "hgvs_p": null,
          "transcript": "NM_001284297.2",
          "protein_id": "NP_001271226.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1181,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3546,
          "cdna_start": null,
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          "cdna_length": 4615,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "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": 31,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "PLCB2",
          "gene_hgnc_id": 9055,
          "hgvs_c": "c.163-70C>G",
          "hgvs_p": null,
          "transcript": "NM_001284298.2",
          "protein_id": "NP_001271227.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1170,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3513,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4582,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "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": "PLCB2",
          "gene_hgnc_id": 9055,
          "hgvs_c": "c.163-70C>G",
          "hgvs_p": null,
          "transcript": "NM_001284299.2",
          "protein_id": "NP_001271228.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 199,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 600,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1788,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 29,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "PLCB2",
          "gene_hgnc_id": 9055,
          "hgvs_c": "n.184-70C>G",
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          "transcript": "ENST00000558588.5",
          "protein_id": null,
          "transcript_support_level": 2,
          "aa_start": null,
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          "aa_length": null,
          "cds_start": -4,
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          "cdna_start": null,
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          "mane_select": null,
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          "feature": null
        },
        {
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          "exon_rank": null,
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          "exon_count": 33,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "PLCB2",
          "gene_hgnc_id": 9055,
          "hgvs_c": "c.163-70C>G",
          "hgvs_p": null,
          "transcript": "XM_017022314.3",
          "protein_id": "XP_016877803.1",
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          "aa_length": 1205,
          "cds_start": -4,
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          "cdna_start": null,
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          "mane_select": null,
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        {
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          "hgvs_c": "c.163-70C>G",
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          "mane_select": null,
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        {
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          "canonical": false,
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          "gene_symbol": "PLCB2",
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          "gene_symbol": "PLCB2",
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