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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: 18-33907464-T-G (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=18&pos=33907464&ref=T&alt=G&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "18",
      "pos": 33907464,
      "ref": "T",
      "alt": "G",
      "effect": "intron_variant",
      "transcript": "ENST00000261592.10",
      "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": 9,
          "intron_rank_end": null,
          "gene_symbol": "NOL4",
          "gene_hgnc_id": 7870,
          "hgvs_c": "c.1543-24040A>C",
          "hgvs_p": null,
          "transcript": "NM_003787.5",
          "protein_id": "NP_003778.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 638,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1917,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5319,
          "mane_select": "ENST00000261592.10",
          "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": 9,
          "intron_rank_end": null,
          "gene_symbol": "NOL4",
          "gene_hgnc_id": 7870,
          "hgvs_c": "c.1543-24040A>C",
          "hgvs_p": null,
          "transcript": "ENST00000261592.10",
          "protein_id": "ENSP00000261592.4",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 638,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1917,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5319,
          "mane_select": "NM_003787.5",
          "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": 9,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "NOL4",
          "gene_hgnc_id": 7870,
          "hgvs_c": "c.1237-24040A>C",
          "hgvs_p": null,
          "transcript": "ENST00000589544.5",
          "protein_id": "ENSP00000465450.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 536,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1611,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2221,
          "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": 10,
          "intron_rank_end": null,
          "gene_symbol": "NOL4",
          "gene_hgnc_id": 7870,
          "hgvs_c": "c.1612-24040A>C",
          "hgvs_p": null,
          "transcript": "NM_001384467.1",
          "protein_id": "NP_001371396.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 661,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1986,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5388,
          "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": 9,
          "intron_rank_end": null,
          "gene_symbol": "NOL4",
          "gene_hgnc_id": 7870,
          "hgvs_c": "c.1420-24040A>C",
          "hgvs_p": null,
          "transcript": "NM_001384468.1",
          "protein_id": "NP_001371397.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 597,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1794,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5196,
          "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": 9,
          "intron_rank_end": null,
          "gene_symbol": "NOL4",
          "gene_hgnc_id": 7870,
          "hgvs_c": "c.1414-24040A>C",
          "hgvs_p": null,
          "transcript": "NM_001384469.1",
          "protein_id": "NP_001371398.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 595,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1788,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5190,
          "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": 10,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "NOL4",
          "gene_hgnc_id": 7870,
          "hgvs_c": "c.1351-24040A>C",
          "hgvs_p": null,
          "transcript": "NM_001198546.1",
          "protein_id": "NP_001185475.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 574,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1725,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3765,
          "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": 9,
          "intron_rank_end": null,
          "gene_symbol": "NOL4",
          "gene_hgnc_id": 7870,
          "hgvs_c": "c.1321-24040A>C",
          "hgvs_p": null,
          "transcript": "NM_001198547.2",
          "protein_id": "NP_001185476.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 564,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1695,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3846,
          "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": 9,
          "intron_rank_end": null,
          "gene_symbol": "NOL4",
          "gene_hgnc_id": 7870,
          "hgvs_c": "c.1321-24040A>C",
          "hgvs_p": null,
          "transcript": "ENST00000538587.5",
          "protein_id": "ENSP00000443472.1",
          "transcript_support_level": 2,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 564,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1695,
          "cdna_start": null,
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          "cdna_length": 1979,
          "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": [
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          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "NOL4",
          "gene_hgnc_id": 7870,
          "hgvs_c": "c.1303-24040A>C",
          "hgvs_p": null,
          "transcript": "ENST00000590712.5",
          "protein_id": "ENSP00000467629.1",
          "transcript_support_level": 2,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 558,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1677,
          "cdna_start": null,
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          "cdna_length": 1930,
          "mane_select": null,
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          "biotype": null,
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        {
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          "canonical": false,
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          "exon_count": 9,
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          "gene_symbol": "NOL4",
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          "transcript": "NM_001198548.1",
          "protein_id": "NP_001185477.1",
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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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          "feature": null
        },
        {
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          "canonical": false,
          "protein_coding": true,
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          "consequences": [
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          "intron_rank": 9,
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          "gene_symbol": "NOL4",
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          "hgvs_p": null,
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        {
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          "gene_symbol": "NOL4",
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          "hgvs_c": "c.1129-24040A>C",
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          "gene_symbol": "NOL4",
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          "transcript": "NM_001353235.2",
          "protein_id": "NP_001340164.1",
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        {
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          "gene_symbol": "NOL4",
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          "transcript": "NM_001282527.2",
          "protein_id": "NP_001269456.1",
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          "gene_symbol": "NOL4",
          "gene_hgnc_id": 7870,
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          "transcript": "NM_001353237.1",
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        },
        {
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        {
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          "gene_symbol": "NOL4",
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          "transcript": "NM_001198549.2",
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          "feature": null
        },
        {
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          "consequences": [
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          ],
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          "exon_count": 13,
          "intron_rank": 11,
          "intron_rank_end": null,
          "gene_symbol": "NOL4",
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          "hgvs_c": "c.688-24040A>C",
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          "transcript": "NM_001384472.1",
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