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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: 10-121812677-G-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=10&pos=121812677&ref=G&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "10",
      "pos": 121812677,
      "ref": "G",
      "alt": "C",
      "effect": "intron_variant",
      "transcript": "ENST00000224652.12",
      "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": 12,
          "intron_rank": 10,
          "intron_rank_end": null,
          "gene_symbol": "ATE1",
          "gene_hgnc_id": 782,
          "hgvs_c": "c.1258-22388C>G",
          "hgvs_p": null,
          "transcript": "NM_001001976.3",
          "protein_id": "NP_001001976.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 518,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1557,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4895,
          "mane_select": "ENST00000224652.12",
          "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": 12,
          "intron_rank": 10,
          "intron_rank_end": null,
          "gene_symbol": "ATE1",
          "gene_hgnc_id": 782,
          "hgvs_c": "c.1258-22388C>G",
          "hgvs_p": null,
          "transcript": "ENST00000224652.12",
          "protein_id": "ENSP00000224652.6",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 518,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1557,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4895,
          "mane_select": "NM_001001976.3",
          "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": 12,
          "intron_rank": 10,
          "intron_rank_end": null,
          "gene_symbol": "ATE1",
          "gene_hgnc_id": 782,
          "hgvs_c": "c.1258-22388C>G",
          "hgvs_p": null,
          "transcript": "ENST00000369043.8",
          "protein_id": "ENSP00000358039.3",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 518,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1557,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4895,
          "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": 10,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "ATE1",
          "gene_hgnc_id": 782,
          "hgvs_c": "n.*975-22388C>G",
          "hgvs_p": null,
          "transcript": "ENST00000423243.7",
          "protein_id": "ENSP00000397787.2",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2040,
          "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": 13,
          "intron_rank": 11,
          "intron_rank_end": null,
          "gene_symbol": "ATE1",
          "gene_hgnc_id": 782,
          "hgvs_c": "c.1438-22388C>G",
          "hgvs_p": null,
          "transcript": "NM_001439361.1",
          "protein_id": "NP_001426290.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 578,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1737,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5426,
          "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": 13,
          "intron_rank": 11,
          "intron_rank_end": null,
          "gene_symbol": "ATE1",
          "gene_hgnc_id": 782,
          "hgvs_c": "c.1387-22388C>G",
          "hgvs_p": null,
          "transcript": "NM_001437419.1",
          "protein_id": "NP_001424348.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 561,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1686,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5024,
          "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": 13,
          "intron_rank": 11,
          "intron_rank_end": null,
          "gene_symbol": "ATE1",
          "gene_hgnc_id": 782,
          "hgvs_c": "c.1387-22388C>G",
          "hgvs_p": null,
          "transcript": "ENST00000690355.1",
          "protein_id": "ENSP00000510433.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 561,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1686,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5059,
          "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": 13,
          "intron_rank": 11,
          "intron_rank_end": null,
          "gene_symbol": "ATE1",
          "gene_hgnc_id": 782,
          "hgvs_c": "c.1372-22388C>G",
          "hgvs_p": null,
          "transcript": "ENST00000687089.1",
          "protein_id": "ENSP00000510151.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 556,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1671,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5044,
          "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": 13,
          "intron_rank": 11,
          "intron_rank_end": null,
          "gene_symbol": "ATE1",
          "gene_hgnc_id": 782,
          "hgvs_c": "c.1366-22388C>G",
          "hgvs_p": null,
          "transcript": "NM_001439362.1",
          "protein_id": "NP_001426291.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 554,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1665,
          "cdna_start": null,
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          "cdna_length": 4953,
          "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,
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          "exon_count": 12,
          "intron_rank": 10,
          "intron_rank_end": null,
          "gene_symbol": "ATE1",
          "gene_hgnc_id": 782,
          "hgvs_c": "c.1354-22388C>G",
          "hgvs_p": null,
          "transcript": "NM_001439363.1",
          "protein_id": "NP_001426292.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 550,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1653,
          "cdna_start": null,
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          "cdna_length": 4991,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          "intron_rank": 10,
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          "gene_symbol": "ATE1",
          "gene_hgnc_id": 782,
          "hgvs_c": "c.1333-22388C>G",
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          "transcript": "NM_001439364.1",
          "protein_id": "NP_001426293.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 543,
          "cds_start": -4,
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          "cdna_start": null,
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          "cdna_length": 4920,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
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          "strand": false,
          "consequences": [
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          "exon_rank": null,
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          "exon_count": 13,
          "intron_rank": 11,
          "intron_rank_end": null,
          "gene_symbol": "ATE1",
          "gene_hgnc_id": 782,
          "hgvs_c": "c.1330-22388C>G",
          "hgvs_p": null,
          "transcript": "ENST00000691830.1",
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        {
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          "gene_symbol": "ATE1",
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        {
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          "gene_symbol": "ATE1",
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          "hgvs_c": "c.1309-22388C>G",
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        {
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          "gene_symbol": "ATE1",
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        {
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          "gene_symbol": "ATE1",
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          "hgvs_c": "c.1258-22388C>G",
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          "gene_symbol": "ATE1",
          "gene_hgnc_id": 782,
          "hgvs_c": "c.1258-22388C>G",
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        {
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          "intron_rank": 9,
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          "gene_symbol": "ATE1",
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        {
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          "exon_count": 12,
          "intron_rank": 10,
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          "gene_symbol": "ATE1",
          "gene_hgnc_id": 782,
          "hgvs_c": "c.1237-22388C>G",
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          "transcript": "ENST00000540606.7",
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