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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: 1-108941353-T-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=1&pos=108941353&ref=T&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "1",
      "pos": 108941353,
      "ref": "T",
      "alt": "C",
      "effect": "intron_variant",
      "transcript": "ENST00000369969.7",
      "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": 13,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "CLCC1",
          "gene_hgnc_id": 29675,
          "hgvs_c": "c.796+52A>G",
          "hgvs_p": null,
          "transcript": "NM_001377458.1",
          "protein_id": "NP_001364387.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 551,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1656,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4994,
          "mane_select": "ENST00000369969.7",
          "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": 13,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "CLCC1",
          "gene_hgnc_id": 29675,
          "hgvs_c": "c.796+52A>G",
          "hgvs_p": null,
          "transcript": "ENST00000369969.7",
          "protein_id": "ENSP00000358986.3",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 551,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1656,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4994,
          "mane_select": "NM_001377458.1",
          "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": 11,
          "intron_rank": 6,
          "intron_rank_end": null,
          "gene_symbol": "CLCC1",
          "gene_hgnc_id": 29675,
          "hgvs_c": "c.433+52A>G",
          "hgvs_p": null,
          "transcript": "ENST00000302500.5",
          "protein_id": "ENSP00000306552.4",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 430,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1293,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1708,
          "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": 6,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "CLCC1",
          "gene_hgnc_id": 29675,
          "hgvs_c": "c.340-1571A>G",
          "hgvs_p": null,
          "transcript": "ENST00000348264.6",
          "protein_id": "ENSP00000337243.2",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 366,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1101,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1124,
          "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": 14,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "CLCC1",
          "gene_hgnc_id": 29675,
          "hgvs_c": "c.796+52A>G",
          "hgvs_p": null,
          "transcript": "ENST00000676392.2",
          "protein_id": "ENSP00000501566.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 568,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1707,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2407,
          "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": 12,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "CLCC1",
          "gene_hgnc_id": 29675,
          "hgvs_c": "c.796+52A>G",
          "hgvs_p": null,
          "transcript": "NM_001048210.3",
          "protein_id": "NP_001041675.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 551,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1656,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4823,
          "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": 8,
          "intron_rank_end": null,
          "gene_symbol": "CLCC1",
          "gene_hgnc_id": 29675,
          "hgvs_c": "c.796+52A>G",
          "hgvs_p": null,
          "transcript": "NM_001377459.1",
          "protein_id": "NP_001364388.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 551,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1656,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4999,
          "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": 12,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "CLCC1",
          "gene_hgnc_id": 29675,
          "hgvs_c": "c.796+52A>G",
          "hgvs_p": null,
          "transcript": "NM_001377460.1",
          "protein_id": "NP_001364389.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 551,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1656,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4838,
          "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": 12,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "CLCC1",
          "gene_hgnc_id": 29675,
          "hgvs_c": "c.796+52A>G",
          "hgvs_p": null,
          "transcript": "NM_001377461.1",
          "protein_id": "NP_001364390.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 551,
          "cds_start": -4,
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          "cdna_start": null,
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          "cdna_length": 4833,
          "mane_select": null,
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          "feature": null
        },
        {
          "aa_ref": 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": 12,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "CLCC1",
          "gene_hgnc_id": 29675,
          "hgvs_c": "c.796+52A>G",
          "hgvs_p": null,
          "transcript": "NM_001377462.1",
          "protein_id": "NP_001364391.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 551,
          "cds_start": -4,
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          "cdna_start": null,
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          "cdna_length": 4798,
          "mane_select": null,
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        },
        {
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          "exon_count": 12,
          "intron_rank": 7,
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          "gene_symbol": "CLCC1",
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          "hgvs_c": "c.796+52A>G",
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          "aa_start": null,
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          "cds_start": -4,
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          "mane_select": null,
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        {
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          "canonical": false,
          "protein_coding": true,
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          "consequences": [
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          "intron_rank": 7,
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          "gene_symbol": "CLCC1",
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          "hgvs_c": "c.796+52A>G",
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          "gene_symbol": "CLCC1",
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          "hgvs_c": "c.796+52A>G",
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        {
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          "gene_symbol": "CLCC1",
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        {
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