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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: 8-27600587-G-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=8&pos=27600587&ref=G&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "8",
      "pos": 27600587,
      "ref": "G",
      "alt": "C",
      "effect": "intron_variant",
      "transcript": "NM_001831.4",
      "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": 9,
          "intron_rank": 6,
          "intron_rank_end": null,
          "gene_symbol": "CLU",
          "gene_hgnc_id": 2095,
          "hgvs_c": "c.935-578C>G",
          "hgvs_p": null,
          "transcript": "NM_001831.4",
          "protein_id": "NP_001822.3",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 449,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1350,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2749,
          "mane_select": "ENST00000316403.15",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001831.4"
        },
        {
          "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": 9,
          "intron_rank": 6,
          "intron_rank_end": null,
          "gene_symbol": "CLU",
          "gene_hgnc_id": 2095,
          "hgvs_c": "c.935-578C>G",
          "hgvs_p": null,
          "transcript": "ENST00000316403.15",
          "protein_id": "ENSP00000315130.10",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 449,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1350,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2749,
          "mane_select": "NM_001831.4",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000316403.15"
        },
        {
          "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": 9,
          "intron_rank": 6,
          "intron_rank_end": null,
          "gene_symbol": "CLU",
          "gene_hgnc_id": 2095,
          "hgvs_c": "c.935-578C>G",
          "hgvs_p": null,
          "transcript": "ENST00000405140.7",
          "protein_id": "ENSP00000385419.3",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 449,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1350,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2098,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000405140.7"
        },
        {
          "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": 5,
          "intron_rank_end": null,
          "gene_symbol": "CLU",
          "gene_hgnc_id": 2095,
          "hgvs_c": "c.935-578C>G",
          "hgvs_p": null,
          "transcript": "ENST00000523500.5",
          "protein_id": "ENSP00000429620.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 449,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1350,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2381,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000523500.5"
        },
        {
          "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": 10,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "CLU",
          "gene_hgnc_id": 2095,
          "hgvs_c": "c.935-578C>G",
          "hgvs_p": null,
          "transcript": "ENST00000877517.1",
          "protein_id": "ENSP00000547576.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 449,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1350,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2058,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000877517.1"
        },
        {
          "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": 10,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "CLU",
          "gene_hgnc_id": 2095,
          "hgvs_c": "c.935-578C>G",
          "hgvs_p": null,
          "transcript": "ENST00000877518.1",
          "protein_id": "ENSP00000547577.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 449,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1350,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2060,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000877518.1"
        },
        {
          "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": 9,
          "intron_rank": 6,
          "intron_rank_end": null,
          "gene_symbol": "CLU",
          "gene_hgnc_id": 2095,
          "hgvs_c": "c.935-578C>G",
          "hgvs_p": null,
          "transcript": "ENST00000877520.1",
          "protein_id": "ENSP00000547579.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 449,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1350,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1674,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000877520.1"
        },
        {
          "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": 10,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "CLU",
          "gene_hgnc_id": 2095,
          "hgvs_c": "c.935-578C>G",
          "hgvs_p": null,
          "transcript": "ENST00000877521.1",
          "protein_id": "ENSP00000547580.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 449,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1350,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1781,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000877521.1"
        },
        {
          "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": 9,
          "intron_rank": 6,
          "intron_rank_end": null,
          "gene_symbol": "CLU",
          "gene_hgnc_id": 2095,
          "hgvs_c": "c.935-578C>G",
          "hgvs_p": null,
          "transcript": "ENST00000877522.1",
          "protein_id": "ENSP00000547581.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 449,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1350,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1706,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000877522.1"
        },
        {
          "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": 10,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "CLU",
          "gene_hgnc_id": 2095,
          "hgvs_c": "c.935-578C>G",
          "hgvs_p": null,
          "transcript": "ENST00000877523.1",
          "protein_id": "ENSP00000547582.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 449,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1350,
          "cdna_start": null,
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          "cdna_length": 1693,
          "mane_select": null,
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          "biotype": "protein_coding",
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        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
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          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 10,
          "intron_rank": 7,
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          "gene_symbol": "CLU",
          "gene_hgnc_id": 2095,
          "hgvs_c": "c.935-578C>G",
          "hgvs_p": null,
          "transcript": "ENST00000877524.1",
          "protein_id": "ENSP00000547583.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 449,
          "cds_start": null,
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          "cds_length": 1350,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1778,
          "mane_select": null,
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          "biotype": "protein_coding",
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        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
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          "exon_count": 9,
          "intron_rank": 6,
          "intron_rank_end": null,
          "gene_symbol": "CLU",
          "gene_hgnc_id": 2095,
          "hgvs_c": "c.935-578C>G",
          "hgvs_p": null,
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          "protein_id": "ENSP00000547584.1",
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          "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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          ],
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          "gene_symbol": "CLU",
          "gene_hgnc_id": 2095,
          "hgvs_c": "c.935-578C>G",
          "hgvs_p": null,
          "transcript": "ENST00000877526.1",
          "protein_id": "ENSP00000547585.1",
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        {
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          "intron_rank": 6,
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          "gene_symbol": "CLU",
          "gene_hgnc_id": 2095,
          "hgvs_c": "c.935-578C>G",
          "hgvs_p": null,
          "transcript": "ENST00000877527.1",
          "protein_id": "ENSP00000547586.1",
          "transcript_support_level": null,
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          "cds_start": null,
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          "mane_select": null,
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        },
        {
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          "gene_symbol": "CLU",
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        {
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          "exon_count": 9,
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          "gene_symbol": "CLU",
          "gene_hgnc_id": 2095,
          "hgvs_c": "c.935-578C>G",
          "hgvs_p": null,
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          "protein_id": "ENSP00000547589.1",
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        {
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          "gene_symbol": "CLU",
          "gene_hgnc_id": 2095,
          "hgvs_c": "c.935-578C>G",
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          "transcript": "ENST00000877531.1",
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        {
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          "gene_symbol": "CLU",
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        {
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          "consequences": [
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          ],
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          "exon_count": 9,
          "intron_rank": 6,
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          "gene_symbol": "CLU",
          "gene_hgnc_id": 2095,
          "hgvs_c": "c.935-578C>G",
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          "transcript": "ENST00000877540.1",
          "protein_id": "ENSP00000547599.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "cdna_start": null,
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          "cdna_length": 1797,
          "mane_select": null,
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          "biotype": "protein_coding",
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        },
        {
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          "consequences": [
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          ],
          "exon_rank": null,
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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.