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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: 12-53601293-T-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=12&pos=53601293&ref=T&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "12",
      "pos": 53601293,
      "ref": "T",
      "alt": "C",
      "effect": "intron_variant",
      "transcript": "NM_001366555.2",
      "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": 1,
          "intron_rank_end": null,
          "gene_symbol": "ATF7",
          "gene_hgnc_id": 792,
          "hgvs_c": "c.-21-272A>G",
          "hgvs_p": null,
          "transcript": "NM_006856.3",
          "protein_id": "NP_006847.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 483,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1452,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 6660,
          "mane_select": "ENST00000420353.7",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_006856.3"
        },
        {
          "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": 1,
          "intron_rank_end": null,
          "gene_symbol": "ATF7",
          "gene_hgnc_id": 792,
          "hgvs_c": "c.-21-272A>G",
          "hgvs_p": null,
          "transcript": "ENST00000420353.7",
          "protein_id": "ENSP00000399465.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 483,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1452,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 6660,
          "mane_select": "NM_006856.3",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000420353.7"
        },
        {
          "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": 1,
          "intron_rank_end": null,
          "gene_symbol": "ATF7-NPFF",
          "gene_hgnc_id": 55073,
          "hgvs_c": "c.-21-272A>G",
          "hgvs_p": null,
          "transcript": "ENST00000591834.1",
          "protein_id": "ENSP00000466174.1",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 463,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1392,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1609,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000591834.1"
        },
        {
          "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": 4,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "ATF7",
          "gene_hgnc_id": 792,
          "hgvs_c": "c.-21-272A>G",
          "hgvs_p": null,
          "transcript": "ENST00000548118.6",
          "protein_id": "ENSP00000456858.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 117,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 354,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 774,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000548118.6"
        },
        {
          "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": 4,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "ATF7",
          "gene_hgnc_id": 792,
          "hgvs_c": "c.-21-272A>G",
          "hgvs_p": null,
          "transcript": "ENST00000591397.1",
          "protein_id": "ENSP00000465192.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 117,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 354,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 860,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000591397.1"
        },
        {
          "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": 12,
          "intron_rank": 1,
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          "gene_symbol": "ATF7",
          "gene_hgnc_id": 792,
          "hgvs_c": "c.-21-272A>G",
          "hgvs_p": null,
          "transcript": "ENST00000923853.1",
          "protein_id": "ENSP00000593912.1",
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          "cds_start": null,
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          "cdna_length": 6702,
          "mane_select": null,
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          "feature": "ENST00000923853.1"
        },
        {
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          "strand": false,
          "consequences": [
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          "exon_count": 12,
          "intron_rank": 1,
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          "gene_symbol": "ATF7",
          "gene_hgnc_id": 792,
          "hgvs_c": "c.-21-272A>G",
          "hgvs_p": null,
          "transcript": "NM_001366555.2",
          "protein_id": "NP_001353484.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "cds_start": null,
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          "cds_length": 1485,
          "cdna_start": null,
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          "cdna_length": 6693,
          "mane_select": null,
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          "biotype": "protein_coding",
          "feature": "NM_001366555.2"
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        {
          "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": 1,
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          "gene_symbol": "ATF7",
          "gene_hgnc_id": 792,
          "hgvs_c": "c.-21-272A>G",
          "hgvs_p": null,
          "transcript": "ENST00000548446.6",
          "protein_id": "ENSP00000449938.1",
          "transcript_support_level": 2,
          "aa_start": null,
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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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        {
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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.