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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: 7-127035332-A-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=7&pos=127035332&ref=A&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "7",
      "pos": 127035332,
      "ref": "A",
      "alt": "C",
      "effect": "intron_variant",
      "transcript": "ENST00000339582.7",
      "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": 11,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "GRM8",
          "gene_hgnc_id": 4600,
          "hgvs_c": "c.727+71164T>G",
          "hgvs_p": null,
          "transcript": "NM_000845.3",
          "protein_id": "NP_000836.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 908,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2727,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3704,
          "mane_select": "ENST00000339582.7",
          "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": 11,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "GRM8",
          "gene_hgnc_id": 4600,
          "hgvs_c": "c.727+71164T>G",
          "hgvs_p": null,
          "transcript": "ENST00000339582.7",
          "protein_id": "ENSP00000344173.2",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 908,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2727,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3704,
          "mane_select": "NM_000845.3",
          "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": 11,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "GRM8",
          "gene_hgnc_id": 4600,
          "hgvs_c": "c.727+71164T>G",
          "hgvs_p": null,
          "transcript": "ENST00000358373.8",
          "protein_id": "ENSP00000351142.3",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 908,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2727,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3741,
          "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": 11,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "GRM8",
          "gene_hgnc_id": 4600,
          "hgvs_c": "n.727+71164T>G",
          "hgvs_p": null,
          "transcript": "ENST00000341617.7",
          "protein_id": "ENSP00000345747.3",
          "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": 3240,
          "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": 3,
          "intron_rank_end": null,
          "gene_symbol": "GRM8",
          "gene_hgnc_id": 4600,
          "hgvs_c": "c.727+71164T>G",
          "hgvs_p": null,
          "transcript": "NM_001371086.1",
          "protein_id": "NP_001358015.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 928,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2787,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3723,
          "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": 3,
          "intron_rank_end": null,
          "gene_symbol": "GRM8",
          "gene_hgnc_id": 4600,
          "hgvs_c": "c.727+71164T>G",
          "hgvs_p": null,
          "transcript": "ENST00000706915.1",
          "protein_id": "ENSP00000516623.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 928,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2787,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3847,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "GRM8",
          "gene_hgnc_id": 4600,
          "hgvs_c": "c.727+71164T>G",
          "hgvs_p": null,
          "transcript": "NM_001127323.1",
          "protein_id": "NP_001120795.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 908,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2727,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3860,
          "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": 4,
          "intron_rank_end": null,
          "gene_symbol": "GRM8",
          "gene_hgnc_id": 4600,
          "hgvs_c": "c.727+71164T>G",
          "hgvs_p": null,
          "transcript": "NM_001371083.1",
          "protein_id": "NP_001358012.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 908,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2727,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3808,
          "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": 11,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "GRM8",
          "gene_hgnc_id": 4600,
          "hgvs_c": "c.727+71164T>G",
          "hgvs_p": null,
          "transcript": "NM_001371084.1",
          "protein_id": "NP_001358013.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "cds_start": -4,
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          "cds_length": 2727,
          "cdna_start": null,
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          "cdna_length": 3686,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
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          "canonical": false,
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          "strand": false,
          "consequences": [
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          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "GRM8",
          "gene_hgnc_id": 4600,
          "hgvs_c": "c.727+71164T>G",
          "hgvs_p": null,
          "transcript": "NM_001371085.1",
          "protein_id": "NP_001358014.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 908,
          "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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          "gene_symbol": "GRM8",
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          "transcript": "ENST00000706916.1",
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          "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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          "intron_rank": 4,
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          "gene_symbol": "GRM8",
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        {
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}