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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: 2-37234643-C-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=37234643&ref=C&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "2",
      "pos": 37234643,
      "ref": "C",
      "alt": "A",
      "effect": "intron_variant",
      "transcript": "NM_144736.5",
      "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": 10,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "NDUFAF7",
          "gene_hgnc_id": 28816,
          "hgvs_c": "c.217-1453C>A",
          "hgvs_p": null,
          "transcript": "NM_144736.5",
          "protein_id": "NP_653337.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 441,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1326,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000002125.9",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_144736.5"
        },
        {
          "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": 10,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "NDUFAF7",
          "gene_hgnc_id": 28816,
          "hgvs_c": "c.217-1453C>A",
          "hgvs_p": null,
          "transcript": "ENST00000002125.9",
          "protein_id": "ENSP00000002125.4",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 441,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1326,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_144736.5",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000002125.9"
        },
        {
          "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": 8,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "NDUFAF7",
          "gene_hgnc_id": 28816,
          "hgvs_c": "c.216+2377C>A",
          "hgvs_p": null,
          "transcript": "ENST00000336237.10",
          "protein_id": "ENSP00000337431.6",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 343,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1032,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000336237.10"
        },
        {
          "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": 10,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "NDUFAF7",
          "gene_hgnc_id": 28816,
          "hgvs_c": "c.217-1453C>A",
          "hgvs_p": null,
          "transcript": "ENST00000885393.1",
          "protein_id": "ENSP00000555452.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 425,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1278,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000885393.1"
        },
        {
          "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": 9,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "NDUFAF7",
          "gene_hgnc_id": 28816,
          "hgvs_c": "c.216+2377C>A",
          "hgvs_p": null,
          "transcript": "ENST00000885394.1",
          "protein_id": "ENSP00000555453.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 414,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1245,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000885394.1"
        },
        {
          "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": 10,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "NDUFAF7",
          "gene_hgnc_id": 28816,
          "hgvs_c": "c.217-1453C>A",
          "hgvs_p": null,
          "transcript": "NM_001350024.2",
          "protein_id": "NP_001336953.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 400,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1203,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001350024.2"
        },
        {
          "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": 9,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "NDUFAF7",
          "gene_hgnc_id": 28816,
          "hgvs_c": "c.216+2377C>A",
          "hgvs_p": null,
          "transcript": "NM_001350025.2",
          "protein_id": "NP_001336954.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 373,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1122,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001350025.2"
        },
        {
          "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": 9,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "NDUFAF7",
          "gene_hgnc_id": 28816,
          "hgvs_c": "c.217-1453C>A",
          "hgvs_p": null,
          "transcript": "NM_001350027.2",
          "protein_id": "NP_001336956.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 370,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1113,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001350027.2"
        },
        {
          "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": 9,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "NDUFAF7",
          "gene_hgnc_id": 28816,
          "hgvs_c": "c.217-1453C>A",
          "hgvs_p": null,
          "transcript": "ENST00000885392.1",
          "protein_id": "ENSP00000555451.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 370,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1113,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000885392.1"
        },
        {
          "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": 9,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "NDUFAF7",
          "gene_hgnc_id": 28816,
          "hgvs_c": "c.217-1453C>A",
          "hgvs_p": null,
          "transcript": "ENST00000885396.1",
          "protein_id": "ENSP00000555455.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 359,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1080,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
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          "biotype": "protein_coding",
          "feature": "ENST00000885396.1"
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": null,
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          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "NDUFAF7",
          "gene_hgnc_id": 28816,
          "hgvs_c": "c.217-1453C>A",
          "hgvs_p": null,
          "transcript": "ENST00000885395.1",
          "protein_id": "ENSP00000555454.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 354,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1065,
          "cdna_start": null,
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          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000885395.1"
        },
        {
          "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": 8,
          "intron_rank": 2,
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          "gene_symbol": "NDUFAF7",
          "gene_hgnc_id": 28816,
          "hgvs_c": "c.216+2377C>A",
          "hgvs_p": null,
          "transcript": "NM_001083946.2",
          "protein_id": "NP_001077415.1",
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          "cds_start": null,
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          "cdna_start": null,
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          "biotype": "protein_coding",
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        },
        {
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          "canonical": false,
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          "consequences": [
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          ],
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          "intron_rank": 2,
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          "gene_symbol": "NDUFAF7",
          "gene_hgnc_id": 28816,
          "hgvs_c": "c.217-1453C>A",
          "hgvs_p": null,
          "transcript": "ENST00000953410.1",
          "protein_id": "ENSP00000623469.1",
          "transcript_support_level": null,
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          "cds_start": null,
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        {
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          "canonical": false,
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          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "NDUFAF7",
          "gene_hgnc_id": 28816,
          "hgvs_c": "c.217-1453C>A",
          "hgvs_p": null,
          "transcript": "ENST00000934435.1",
          "protein_id": "ENSP00000604493.1",
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          "cds_start": null,
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          "cdna_start": null,
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        {
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          "protein_id": "ENSP00000394436.1",
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        {
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          ],
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          "exon_count": 7,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "NDUFAF7",
          "gene_hgnc_id": 28816,
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          "hgvs_p": null,
          "transcript": "ENST00000431821.5",
          "protein_id": "ENSP00000399207.1",
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          "aa_start": null,
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        {
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          "exon_count": 5,
          "intron_rank": 2,
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          "gene_symbol": "NDUFAF7",
          "gene_hgnc_id": 28816,
          "hgvs_c": "c.91-1453C>A",
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          "transcript": "ENST00000432075.1",
          "protein_id": "ENSP00000402959.1",
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          "transcript": "ENST00000416653.5",
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        {
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        {
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          "consequences": [
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          ],
          "exon_rank": null,
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          "exon_count": 9,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "NDUFAF7",
          "gene_hgnc_id": 28816,
          "hgvs_c": "c.91-1453C>A",
          "hgvs_p": null,
          "transcript": "XM_024452977.2",
          "protein_id": "XP_024308745.1",
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          "aa_length": 328,
          "cds_start": null,
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          "cds_length": 987,
          "cdna_start": null,
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          "cdna_length": null,
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          "biotype": "protein_coding",
          "feature": "XM_024452977.2"
        },
        {
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          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
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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.