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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: 20-35717523-C-G (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=20&pos=35717523&ref=C&alt=G&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "20",
      "pos": 35717523,
      "ref": "C",
      "alt": "G",
      "effect": "intron_variant",
      "transcript": "ENST00000253363.11",
      "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": 17,
          "intron_rank": 9,
          "intron_rank_end": null,
          "gene_symbol": "RBM39",
          "gene_hgnc_id": 15923,
          "hgvs_c": "c.826-718G>C",
          "hgvs_p": null,
          "transcript": "NM_184234.3",
          "protein_id": "NP_909122.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 530,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1593,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5060,
          "mane_select": "ENST00000253363.11",
          "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": 17,
          "intron_rank": 9,
          "intron_rank_end": null,
          "gene_symbol": "RBM39",
          "gene_hgnc_id": 15923,
          "hgvs_c": "c.826-718G>C",
          "hgvs_p": null,
          "transcript": "ENST00000253363.11",
          "protein_id": "ENSP00000253363.6",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 530,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1593,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5060,
          "mane_select": "NM_184234.3",
          "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": 17,
          "intron_rank": 9,
          "intron_rank_end": null,
          "gene_symbol": "RBM39",
          "gene_hgnc_id": 15923,
          "hgvs_c": "c.826-718G>C",
          "hgvs_p": null,
          "transcript": "ENST00000361162.10",
          "protein_id": "ENSP00000354437.6",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 524,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1575,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2831,
          "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": 16,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "RBM39",
          "gene_hgnc_id": 15923,
          "hgvs_c": "c.760-718G>C",
          "hgvs_p": null,
          "transcript": "ENST00000528062.7",
          "protein_id": "ENSP00000436747.2",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 508,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1527,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2421,
          "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": 17,
          "intron_rank": 9,
          "intron_rank_end": null,
          "gene_symbol": "RBM39",
          "gene_hgnc_id": 15923,
          "hgvs_c": "c.823-718G>C",
          "hgvs_p": null,
          "transcript": "NM_001323424.2",
          "protein_id": "NP_001310353.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 529,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1590,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5057,
          "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": 17,
          "intron_rank": 9,
          "intron_rank_end": null,
          "gene_symbol": "RBM39",
          "gene_hgnc_id": 15923,
          "hgvs_c": "c.826-718G>C",
          "hgvs_p": null,
          "transcript": "NM_004902.4",
          "protein_id": "NP_004893.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 524,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1575,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5042,
          "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": 16,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "RBM39",
          "gene_hgnc_id": 15923,
          "hgvs_c": "c.760-718G>C",
          "hgvs_p": null,
          "transcript": "NM_001242599.2",
          "protein_id": "NP_001229528.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 508,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1527,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4994,
          "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": 16,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "RBM39",
          "gene_hgnc_id": 15923,
          "hgvs_c": "c.760-718G>C",
          "hgvs_p": null,
          "transcript": "NM_001242600.2",
          "protein_id": "NP_001229529.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 502,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1509,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4976,
          "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": 16,
          "intron_rank": 9,
          "intron_rank_end": null,
          "gene_symbol": "RBM39",
          "gene_hgnc_id": 15923,
          "hgvs_c": "c.826-718G>C",
          "hgvs_p": null,
          "transcript": "NM_001323422.2",
          "protein_id": "NP_001310351.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 498,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1497,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4964,
          "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": 19,
          "intron_rank": 11,
          "intron_rank_end": null,
          "gene_symbol": "RBM39",
          "gene_hgnc_id": 15923,
          "hgvs_c": "c.355-718G>C",
          "hgvs_p": null,
          "transcript": "NM_001323423.2",
          "protein_id": "NP_001310352.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 373,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1122,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5205,
          "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": 4,
          "intron_rank_end": null,
          "gene_symbol": "RBM39",
          "gene_hgnc_id": 15923,
          "hgvs_c": "c.442-3134G>C",
          "hgvs_p": null,
          "transcript": "ENST00000448303.5",
          "protein_id": "ENSP00000394824.1",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 334,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1007,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1008,
          "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": 18,
          "intron_rank": 9,
          "intron_rank_end": null,
          "gene_symbol": "RBM39",
          "gene_hgnc_id": 15923,
          "hgvs_c": "n.826-718G>C",
          "hgvs_p": null,
          "transcript": "ENST00000338163.10",
          "protein_id": "ENSP00000344581.6",
          "transcript_support_level": 2,
          "aa_start": null,
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          "aa_length": null,
          "cds_start": -4,
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          "mane_select": null,
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          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
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          "strand": false,
          "consequences": [
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          ],
          "exon_rank": null,
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          "exon_count": 18,
          "intron_rank": 10,
          "intron_rank_end": null,
          "gene_symbol": "RBM39",
          "gene_hgnc_id": 15923,
          "hgvs_c": "n.*776-718G>C",
          "hgvs_p": null,
          "transcript": "ENST00000403542.6",
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          "aa_start": null,
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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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          "biotype": null,
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        },
        {
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          "exon_count": 18,
          "intron_rank": 10,
          "intron_rank_end": null,
          "gene_symbol": "RBM39",
          "gene_hgnc_id": 15923,
          "hgvs_c": "n.*754-718G>C",
          "hgvs_p": null,
          "transcript": "ENST00000429968.5",
          "protein_id": "ENSP00000395124.1",
          "transcript_support_level": 2,
          "aa_start": null,
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          "aa_length": null,
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          "mane_select": null,
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        },
        {
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          "canonical": false,
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          "consequences": [
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          "intron_rank": 10,
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          "gene_symbol": "RBM39",
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          "hgvs_c": "n.*776-718G>C",
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        {
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          "intron_rank": 7,
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          "gene_symbol": "RBM39",
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          "hgvs_c": "n.795-718G>C",
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          "transcript": "ENST00000461283.5",
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          "mane_select": null,
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          "feature": null
        },
        {
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          "strand": false,
          "consequences": [
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          ],
          "exon_rank": null,
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          "exon_count": 16,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "RBM39",
          "gene_hgnc_id": 15923,
          "hgvs_c": "n.2941-718G>C",
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          "transcript": "ENST00000463004.5",
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        },
        {
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          "canonical": false,
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          "strand": false,
          "consequences": [
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          ],
          "exon_rank": null,
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          "exon_count": 7,
          "intron_rank": 3,
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          "gene_symbol": "RBM39",
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          "hgvs_c": "n.367-718G>C",
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          "transcript": "ENST00000490484.7",
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          "gene_symbol": "RBM39",
          "gene_hgnc_id": 15923,
          "hgvs_c": "n.1396-718G>C",
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        {
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          ],
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          "exon_count": 7,
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          "gene_symbol": "RBM39",
          "gene_hgnc_id": 15923,
          "hgvs_c": "n.318-718G>C",
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          "transcript": "ENST00000494274.5",
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          "cdna_length": 704,
          "mane_select": null,
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        },
        {
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          "canonical": false,
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          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "RBM39",
          "gene_hgnc_id": 15923,
          "hgvs_c": "n.100-718G>C",
          "hgvs_p": null,
          "transcript": "ENST00000615771.5",
          "protein_id": "ENSP00000489196.1",
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          "cdna_start": null,
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          "cdna_length": 686,
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}