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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: 10-69333636-C-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=10&pos=69333636&ref=C&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "10",
      "pos": 69333636,
      "ref": "C",
      "alt": "T",
      "effect": "intron_variant",
      "transcript": "ENST00000359426.7",
      "consequences": [
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "HK1",
          "gene_hgnc_id": 4922,
          "hgvs_c": "c.76-10191C>T",
          "hgvs_p": null,
          "transcript": "NM_001358263.1",
          "protein_id": "NP_001345192.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 921,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2766,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3998,
          "mane_select": null,
          "mane_plus": "ENST00000643399.2",
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "HK1",
          "gene_hgnc_id": 4922,
          "hgvs_c": "c.76-10191C>T",
          "hgvs_p": null,
          "transcript": "ENST00000643399.2",
          "protein_id": "ENSP00000494664.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 921,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2766,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3998,
          "mane_select": null,
          "mane_plus": "NM_001358263.1",
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "HK1",
          "gene_hgnc_id": 4922,
          "hgvs_c": "c.64-10191C>T",
          "hgvs_p": null,
          "transcript": "NM_000188.3",
          "protein_id": "NP_000179.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 917,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2754,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3602,
          "mane_select": "ENST00000359426.7",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "HK1",
          "gene_hgnc_id": 4922,
          "hgvs_c": "c.64-10191C>T",
          "hgvs_p": null,
          "transcript": "ENST00000359426.7",
          "protein_id": "ENSP00000352398.6",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 917,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2754,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3602,
          "mane_select": "NM_000188.3",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": 6,
          "intron_rank_end": null,
          "gene_symbol": "HK1",
          "gene_hgnc_id": 4922,
          "hgvs_c": "c.169-10191C>T",
          "hgvs_p": null,
          "transcript": "ENST00000464803.6",
          "protein_id": "ENSP00000496531.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 58,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 178,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 567,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "HK1",
          "gene_hgnc_id": 4922,
          "hgvs_c": "n.380-4862C>T",
          "hgvs_p": null,
          "transcript": "ENST00000480047.5",
          "protein_id": null,
          "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": 575,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": 6,
          "intron_rank_end": null,
          "gene_symbol": "HK1",
          "gene_hgnc_id": 4922,
          "hgvs_c": "c.169-10191C>T",
          "hgvs_p": null,
          "transcript": "NM_001322365.2",
          "protein_id": "NP_001309294.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 952,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2859,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3995,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "HK1",
          "gene_hgnc_id": 4922,
          "hgvs_c": "c.76-10191C>T",
          "hgvs_p": null,
          "transcript": "NM_001322364.2",
          "protein_id": "NP_001309293.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 921,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2766,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3690,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "HK1",
          "gene_hgnc_id": 4922,
          "hgvs_c": "c.76-10191C>T",
          "hgvs_p": null,
          "transcript": "NM_033497.3",
          "protein_id": "NP_277032.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 921,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2766,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3812,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "HK1",
          "gene_hgnc_id": 4922,
          "hgvs_c": "c.76-10191C>T",
          "hgvs_p": null,
          "transcript": "NM_033498.3",
          "protein_id": "NP_277033.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 921,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2766,
          "cdna_start": null,
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          "cdna_length": 3866,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": null,
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          "exon_count": 21,
          "intron_rank": 4,
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          "gene_symbol": "HK1",
          "gene_hgnc_id": 4922,
          "hgvs_c": "c.76-10191C>T",
          "hgvs_p": null,
          "transcript": "ENST00000436817.6",
          "protein_id": "ENSP00000415949.2",
          "transcript_support_level": 5,
          "aa_start": null,
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          "aa_length": 921,
          "cds_start": -4,
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          "cds_length": 2766,
          "cdna_start": null,
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          "cdna_length": 3835,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": null,
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          "exon_count": 18,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "HK1",
          "gene_hgnc_id": 4922,
          "hgvs_c": "c.64-10191C>T",
          "hgvs_p": null,
          "transcript": "NM_001441139.1",
          "protein_id": "NP_001428068.1",
          "transcript_support_level": null,
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        {
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          "exon_count": 18,
          "intron_rank": 1,
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          "gene_symbol": "HK1",
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          "hgvs_c": "c.61-10191C>T",
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          "mane_select": null,
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        {
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          "intron_rank": 1,
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          "gene_symbol": "HK1",
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          "hgvs_c": "c.61-10191C>T",
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          "transcript": "ENST00000298649.8",
          "protein_id": "ENSP00000298649.3",
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          "aa_length": 916,
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          "mane_select": null,
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        {
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          "gene_symbol": "HK1",
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          "gene_symbol": "HK1",
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          "hgvs_c": "c.64-10191C>T",
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          "transcript": "NM_001441141.1",
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          "intron_rank": 5,
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          "gene_symbol": "HK1",
          "gene_hgnc_id": 4922,
          "hgvs_c": "c.28-10191C>T",
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          "transcript": "NM_033500.2",
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        {
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          "strand": true,
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          ],
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          "intron_rank": 1,
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          "gene_symbol": "HK1",
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          "gene_symbol": "HK1",
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          "gene_symbol": "HK1",
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          "hgvs_c": "c.-21-10191C>T",
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          "mane_select": null,
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        },
        {
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          ],
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          "exon_count": 17,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "HK1",
          "gene_hgnc_id": 4922,
          "hgvs_c": "c.64-10191C>T",
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          "transcript": "NM_001322367.1",
          "protein_id": "NP_001309296.1",
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}