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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: 2-151839271-T-G (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=151839271&ref=T&alt=G&genome=hg38&allGenes=true"

API Response

json
{
  "message": null,
  "variants": [
    {
      "acmg_by_gene": [
        {
          "benign_score": 4,
          "criteria": [
            "PM2",
            "BP4_Strong"
          ],
          "effects": [
            "synonymous_variant"
          ],
          "gene_symbol": "CACNB4",
          "hgnc_id": 1404,
          "hgvs_c": "c.1411A>C",
          "hgvs_p": "p.Arg471Arg",
          "inheritance_mode": "AD",
          "pathogenic_score": 2,
          "score": -2,
          "transcript": "NM_000726.5",
          "verdict": "Likely_benign"
        },
        {
          "benign_score": 4,
          "criteria": [
            "PM2",
            "BP4_Strong"
          ],
          "effects": [
            "intron_variant"
          ],
          "gene_symbol": "ENSG00000283228",
          "hgnc_id": null,
          "hgvs_c": "n.*332+2632A>C",
          "hgvs_p": null,
          "inheritance_mode": "",
          "pathogenic_score": 2,
          "score": -2,
          "transcript": "ENST00000637559.1",
          "verdict": "Likely_benign"
        }
      ],
      "acmg_classification": "Likely_benign",
      "acmg_criteria": "PM2,BP4_Strong",
      "acmg_score": -2,
      "allele_count_reference_population": 0,
      "alphamissense_prediction": null,
      "alphamissense_score": null,
      "alt": "G",
      "apogee2_prediction": null,
      "apogee2_score": null,
      "bayesdelnoaf_prediction": "Benign",
      "bayesdelnoaf_score": -0.47,
      "chr": "2",
      "clinvar_classification": "",
      "clinvar_disease": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "computational_prediction_selected": "Benign",
      "computational_score_selected": -0.4699999988079071,
      "computational_source_selected": "BayesDel_noAF",
      "consequences": [
        {
          "aa_alt": "R",
          "aa_end": null,
          "aa_length": 520,
          "aa_ref": "R",
          "aa_start": 471,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 7944,
          "cdna_start": 1444,
          "cds_end": null,
          "cds_length": 1563,
          "cds_start": 1411,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 14,
          "exon_rank": 14,
          "exon_rank_end": null,
          "feature": "NM_000726.5",
          "gene_hgnc_id": 1404,
          "gene_symbol": "CACNB4",
          "hgvs_c": "c.1411A>C",
          "hgvs_p": "p.Arg471Arg",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": "ENST00000539935.7",
          "protein_coding": true,
          "protein_id": "NP_000717.2",
          "strand": false,
          "transcript": "NM_000726.5",
          "transcript_support_level": null
        },
        {
          "aa_alt": "R",
          "aa_end": null,
          "aa_length": 520,
          "aa_ref": "R",
          "aa_start": 471,
          "biotype": "protein_coding",
          "canonical": true,
          "cdna_end": null,
          "cdna_length": 7944,
          "cdna_start": 1444,
          "cds_end": null,
          "cds_length": 1563,
          "cds_start": 1411,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 14,
          "exon_rank": 14,
          "exon_rank_end": null,
          "feature": "ENST00000539935.7",
          "gene_hgnc_id": 1404,
          "gene_symbol": "CACNB4",
          "hgvs_c": "c.1411A>C",
          "hgvs_p": "p.Arg471Arg",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": "NM_000726.5",
          "protein_coding": true,
          "protein_id": "ENSP00000438949.1",
          "strand": false,
          "transcript": "ENST00000539935.7",
          "transcript_support_level": 1
        },
        {
          "aa_alt": "R",
          "aa_end": null,
          "aa_length": 486,
          "aa_ref": "R",
          "aa_start": 437,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 8074,
          "cdna_start": 1574,
          "cds_end": null,
          "cds_length": 1461,
          "cds_start": 1309,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 13,
          "exon_rank": 13,
          "exon_rank_end": null,
          "feature": "ENST00000534999.7",
          "gene_hgnc_id": 1404,
          "gene_symbol": "CACNB4",
          "hgvs_c": "c.1309A>C",
          "hgvs_p": "p.Arg437Arg",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000443893.1",
          "strand": false,
          "transcript": "ENST00000534999.7",
          "transcript_support_level": 1
        },
        {
          "aa_alt": "R",
          "aa_end": null,
          "aa_length": 458,
          "aa_ref": "R",
          "aa_start": 409,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1389,
          "cdna_start": 1237,
          "cds_end": null,
          "cds_length": 1377,
          "cds_start": 1225,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 13,
          "exon_rank": 13,
          "exon_rank_end": null,
          "feature": "ENST00000201943.10",
          "gene_hgnc_id": 1404,
          "gene_symbol": "CACNB4",
          "hgvs_c": "c.1225A>C",
          "hgvs_p": "p.Arg409Arg",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000201943.5",
          "strand": false,
          "transcript": "ENST00000201943.10",
          "transcript_support_level": 1
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": null,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "nonsense_mediated_decay",
          "canonical": true,
          "cdna_end": null,
          "cdna_length": 1373,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": null,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 12,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000637559.1",
          "gene_hgnc_id": null,
          "gene_symbol": "ENSG00000283228",
          "hgvs_c": "n.*332+2632A>C",
          "hgvs_p": null,
          "intron_rank": 10,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": false,
          "protein_id": "ENSP00000489697.1",
          "strand": false,
          "transcript": "ENST00000637559.1",
          "transcript_support_level": 5
        },
        {
          "aa_alt": "R",
          "aa_end": null,
          "aa_length": 502,
          "aa_ref": "R",
          "aa_start": 453,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 7971,
          "cdna_start": 1471,
          "cds_end": null,
          "cds_length": 1509,
          "cds_start": 1357,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 14,
          "exon_rank": 14,
          "exon_rank_end": null,
          "feature": "NM_001005746.4",
          "gene_hgnc_id": 1404,
          "gene_symbol": "CACNB4",
          "hgvs_c": "c.1357A>C",
          "hgvs_p": "p.Arg453Arg",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001005746.1",
          "strand": false,
          "transcript": "NM_001005746.4",
          "transcript_support_level": null
        },
        {
          "aa_alt": "R",
          "aa_end": null,
          "aa_length": 502,
          "aa_ref": "R",
          "aa_start": 453,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4615,
          "cdna_start": 1552,
          "cds_end": null,
          "cds_length": 1509,
          "cds_start": 1357,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 14,
          "exon_rank": 14,
          "exon_rank_end": null,
          "feature": "ENST00000638005.1",
          "gene_hgnc_id": 1404,
          "gene_symbol": "CACNB4",
          "hgvs_c": "c.1357A>C",
          "hgvs_p": "p.Arg453Arg",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000489677.1",
          "strand": false,
          "transcript": "ENST00000638005.1",
          "transcript_support_level": 2
        },
        {
          "aa_alt": "R",
          "aa_end": null,
          "aa_length": 490,
          "aa_ref": "R",
          "aa_start": 441,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 3800,
          "cdna_start": 1735,
          "cds_end": null,
          "cds_length": 1473,
          "cds_start": 1321,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 15,
          "exon_rank": 15,
          "exon_rank_end": null,
          "feature": "ENST00000637762.1",
          "gene_hgnc_id": 1404,
          "gene_symbol": "CACNB4",
          "hgvs_c": "c.1321A>C",
          "hgvs_p": "p.Arg441Arg",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000489876.1",
          "strand": false,
          "transcript": "ENST00000637762.1",
          "transcript_support_level": 5
        },
        {
          "aa_alt": "R",
          "aa_end": null,
          "aa_length": 486,
          "aa_ref": "R",
          "aa_start": 437,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 8074,
          "cdna_start": 1574,
          "cds_end": null,
          "cds_length": 1461,
          "cds_start": 1309,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 13,
          "exon_rank": 13,
          "exon_rank_end": null,
          "feature": "NM_001005747.4",
          "gene_hgnc_id": 1404,
          "gene_symbol": "CACNB4",
          "hgvs_c": "c.1309A>C",
          "hgvs_p": "p.Arg437Arg",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001005747.1",
          "strand": false,
          "transcript": "NM_001005747.4",
          "transcript_support_level": null
        },
        {
          "aa_alt": "R",
          "aa_end": null,
          "aa_length": 479,
          "aa_ref": "R",
          "aa_start": 430,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1776,
          "cdna_start": 1310,
          "cds_end": null,
          "cds_length": 1440,
          "cds_start": 1288,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 13,
          "exon_rank": 13,
          "exon_rank_end": null,
          "feature": "ENST00000427385.6",
          "gene_hgnc_id": 1404,
          "gene_symbol": "CACNB4",
          "hgvs_c": "c.1288A>C",
          "hgvs_p": "p.Arg430Arg",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000410978.2",
          "strand": false,
          "transcript": "ENST00000427385.6",
          "transcript_support_level": 5
        },
        {
          "aa_alt": "R",
          "aa_end": null,
          "aa_length": 473,
          "aa_ref": "R",
          "aa_start": 424,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 8234,
          "cdna_start": 1734,
          "cds_end": null,
          "cds_length": 1422,
          "cds_start": 1270,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 14,
          "exon_rank": 14,
          "exon_rank_end": null,
          "feature": "NM_001320722.3",
          "gene_hgnc_id": 1404,
          "gene_symbol": "CACNB4",
          "hgvs_c": "c.1270A>C",
          "hgvs_p": "p.Arg424Arg",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001307651.1",
          "strand": false,
          "transcript": "NM_001320722.3",
          "transcript_support_level": null
        },
        {
          "aa_alt": "R",
          "aa_end": null,
          "aa_length": 473,
          "aa_ref": "R",
          "aa_start": 424,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 8091,
          "cdna_start": 1591,
          "cds_end": null,
          "cds_length": 1422,
          "cds_start": 1270,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 14,
          "exon_rank": 14,
          "exon_rank_end": null,
          "feature": "NM_001330118.1",
          "gene_hgnc_id": 1404,
          "gene_symbol": "CACNB4",
          "hgvs_c": "c.1270A>C",
          "hgvs_p": "p.Arg424Arg",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001317047.1",
          "strand": false,
          "transcript": "NM_001330118.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "R",
          "aa_end": null,
          "aa_length": 473,
          "aa_ref": "R",
          "aa_start": 424,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2159,
          "cdna_start": 1591,
          "cds_end": null,
          "cds_length": 1422,
          "cds_start": 1270,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 14,
          "exon_rank": 14,
          "exon_rank_end": null,
          "feature": "ENST00000439467.6",
          "gene_hgnc_id": 1404,
          "gene_symbol": "CACNB4",
          "hgvs_c": "c.1270A>C",
          "hgvs_p": "p.Arg424Arg",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000390161.2",
          "strand": false,
          "transcript": "ENST00000439467.6",
          "transcript_support_level": 5
        },
        {
          "aa_alt": "R",
          "aa_end": null,
          "aa_length": 473,
          "aa_ref": "R",
          "aa_start": 424,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 7808,
          "cdna_start": 1505,
          "cds_end": null,
          "cds_length": 1422,
          "cds_start": 1270,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 13,
          "exon_rank": 13,
          "exon_rank_end": null,
          "feature": "ENST00000636598.1",
          "gene_hgnc_id": 1404,
          "gene_symbol": "CACNB4",
          "hgvs_c": "c.1270A>C",
          "hgvs_p": "p.Arg424Arg",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000490247.1",
          "strand": false,
          "transcript": "ENST00000636598.1",
          "transcript_support_level": 5
        },
        {
          "aa_alt": "R",
          "aa_end": null,
          "aa_length": 473,
          "aa_ref": "R",
          "aa_start": 424,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 8188,
          "cdna_start": 1783,
          "cds_end": null,
          "cds_length": 1422,
          "cds_start": 1270,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 14,
          "exon_rank": 14,
          "exon_rank_end": null,
          "feature": "ENST00000637217.1",
          "gene_hgnc_id": 1404,
          "gene_symbol": "CACNB4",
          "hgvs_c": "c.1270A>C",
          "hgvs_p": "p.Arg424Arg",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000490250.1",
          "strand": false,
          "transcript": "ENST00000637217.1",
          "transcript_support_level": 5
        },
        {
          "aa_alt": "R",
          "aa_end": null,
          "aa_length": 472,
          "aa_ref": "R",
          "aa_start": 423,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1885,
          "cdna_start": 1605,
          "cds_end": null,
          "cds_length": 1419,
          "cds_start": 1267,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 13,
          "exon_rank": 13,
          "exon_rank_end": null,
          "feature": "ENST00000360283.11",
          "gene_hgnc_id": 1404,
          "gene_symbol": "CACNB4",
          "hgvs_c": "c.1267A>C",
          "hgvs_p": "p.Arg423Arg",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000353425.8",
          "strand": false,
          "transcript": "ENST00000360283.11",
          "transcript_support_level": 5
        },
        {
          "aa_alt": "R",
          "aa_end": null,
          "aa_length": 461,
          "aa_ref": "R",
          "aa_start": 412,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4232,
          "cdna_start": 1395,
          "cds_end": null,
          "cds_length": 1386,
          "cds_start": 1234,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 13,
          "exon_rank": 13,
          "exon_rank_end": null,
          "feature": "ENST00000636442.1",
          "gene_hgnc_id": 1404,
          "gene_symbol": "CACNB4",
          "hgvs_c": "c.1234A>C",
          "hgvs_p": "p.Arg412Arg",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000489779.1",
          "strand": false,
          "transcript": "ENST00000636442.1",
          "transcript_support_level": 5
        },
        {
          "aa_alt": "R",
          "aa_end": null,
          "aa_length": 458,
          "aa_ref": "R",
          "aa_start": 409,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 7881,
          "cdna_start": 1381,
          "cds_end": null,
          "cds_length": 1377,
          "cds_start": 1225,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 13,
          "exon_rank": 13,
          "exon_rank_end": null,
          "feature": "NM_001145798.2",
          "gene_hgnc_id": 1404,
          "gene_symbol": "CACNB4",
          "hgvs_c": "c.1225A>C",
          "hgvs_p": "p.Arg409Arg",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001139270.1",
          "strand": false,
          "transcript": "NM_001145798.2",
          "transcript_support_level": null
        },
        {
          "aa_alt": "R",
          "aa_end": null,
          "aa_length": 452,
          "aa_ref": "R",
          "aa_start": 403,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 7654,
          "cdna_start": 1292,
          "cds_end": null,
          "cds_length": 1359,
          "cds_start": 1207,
          "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.