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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: 17-44911284-T-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=17&pos=44911284&ref=T&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "17",
      "pos": 44911284,
      "ref": "T",
      "alt": "C",
      "effect": "missense_variant",
      "transcript": "NM_001363846.2",
      "consequences": [
        {
          "aa_ref": "D",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "GFAP",
          "gene_hgnc_id": 4235,
          "hgvs_c": "c.1079A>G",
          "hgvs_p": "p.Asp360Gly",
          "transcript": "NM_002055.5",
          "protein_id": "NP_002046.1",
          "transcript_support_level": null,
          "aa_start": 360,
          "aa_end": null,
          "aa_length": 432,
          "cds_start": 1079,
          "cds_end": null,
          "cds_length": 1299,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000588735.3",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_002055.5"
        },
        {
          "aa_ref": "D",
          "aa_alt": "G",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "GFAP",
          "gene_hgnc_id": 4235,
          "hgvs_c": "c.1079A>G",
          "hgvs_p": "p.Asp360Gly",
          "transcript": "ENST00000588735.3",
          "protein_id": "ENSP00000466598.2",
          "transcript_support_level": 1,
          "aa_start": 360,
          "aa_end": null,
          "aa_length": 432,
          "cds_start": 1079,
          "cds_end": null,
          "cds_length": 1299,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_002055.5",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000588735.3"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "GFAP",
          "gene_hgnc_id": 4235,
          "hgvs_c": "n.232A>G",
          "hgvs_p": null,
          "transcript": "ENST00000585543.6",
          "protein_id": null,
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": null,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "retained_intron",
          "feature": "ENST00000585543.6"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "GFAP",
          "gene_hgnc_id": 4235,
          "hgvs_c": "n.2233A>G",
          "hgvs_p": null,
          "transcript": "ENST00000591327.2",
          "protein_id": null,
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": null,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "retained_intron",
          "feature": "ENST00000591327.2"
        },
        {
          "aa_ref": "D",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "GFAP",
          "gene_hgnc_id": 4235,
          "hgvs_c": "c.1079A>G",
          "hgvs_p": "p.Asp360Gly",
          "transcript": "ENST00000639277.1",
          "protein_id": "ENSP00000492432.1",
          "transcript_support_level": 5,
          "aa_start": 360,
          "aa_end": null,
          "aa_length": 505,
          "cds_start": 1079,
          "cds_end": null,
          "cds_length": 1518,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000639277.1"
        },
        {
          "aa_ref": "D",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "GFAP",
          "gene_hgnc_id": 4235,
          "hgvs_c": "c.1079A>G",
          "hgvs_p": "p.Asp360Gly",
          "transcript": "NM_001363846.2",
          "protein_id": "NP_001350775.1",
          "transcript_support_level": null,
          "aa_start": 360,
          "aa_end": null,
          "aa_length": 472,
          "cds_start": 1079,
          "cds_end": null,
          "cds_length": 1419,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001363846.2"
        },
        {
          "aa_ref": "D",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "GFAP",
          "gene_hgnc_id": 4235,
          "hgvs_c": "c.1079A>G",
          "hgvs_p": "p.Asp360Gly",
          "transcript": "ENST00000253408.11",
          "protein_id": "ENSP00000253408.5",
          "transcript_support_level": 5,
          "aa_start": 360,
          "aa_end": null,
          "aa_length": 472,
          "cds_start": 1079,
          "cds_end": null,
          "cds_length": 1419,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000253408.11"
        },
        {
          "aa_ref": "D",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "GFAP",
          "gene_hgnc_id": 4235,
          "hgvs_c": "c.1079A>G",
          "hgvs_p": "p.Asp360Gly",
          "transcript": "ENST00000867443.1",
          "protein_id": "ENSP00000537502.1",
          "transcript_support_level": null,
          "aa_start": 360,
          "aa_end": null,
          "aa_length": 440,
          "cds_start": 1079,
          "cds_end": null,
          "cds_length": 1323,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000867443.1"
        },
        {
          "aa_ref": "D",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "GFAP",
          "gene_hgnc_id": 4235,
          "hgvs_c": "c.1079A>G",
          "hgvs_p": "p.Asp360Gly",
          "transcript": "NM_001242376.3",
          "protein_id": "NP_001229305.1",
          "transcript_support_level": null,
          "aa_start": 360,
          "aa_end": null,
          "aa_length": 438,
          "cds_start": 1079,
          "cds_end": null,
          "cds_length": 1317,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001242376.3"
        },
        {
          "aa_ref": "D",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "GFAP",
          "gene_hgnc_id": 4235,
          "hgvs_c": "c.1079A>G",
          "hgvs_p": "p.Asp360Gly",
          "transcript": "ENST00000638281.1",
          "protein_id": "ENSP00000491088.1",
          "transcript_support_level": 5,
          "aa_start": 360,
          "aa_end": null,
          "aa_length": 438,
          "cds_start": 1079,
          "cds_end": null,
          "cds_length": 1317,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000638281.1"
        },
        {
          "aa_ref": "D",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "GFAP",
          "gene_hgnc_id": 4235,
          "hgvs_c": "c.1079A>G",
          "hgvs_p": "p.Asp360Gly",
          "transcript": "NM_001131019.3",
          "protein_id": "NP_001124491.1",
          "transcript_support_level": null,
          "aa_start": 360,
          "aa_end": null,
          "aa_length": 431,
          "cds_start": 1079,
          "cds_end": null,
          "cds_length": 1296,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001131019.3"
        },
        {
          "aa_ref": "D",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "GFAP",
          "gene_hgnc_id": 4235,
          "hgvs_c": "c.1079A>G",
          "hgvs_p": "p.Asp360Gly",
          "transcript": "ENST00000435360.8",
          "protein_id": "ENSP00000403962.1",
          "transcript_support_level": 2,
          "aa_start": 360,
          "aa_end": null,
          "aa_length": 431,
          "cds_start": 1079,
          "cds_end": null,
          "cds_length": 1296,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000435360.8"
        },
        {
          "aa_ref": "D",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "GFAP",
          "gene_hgnc_id": 4235,
          "hgvs_c": "c.1076A>G",
          "hgvs_p": "p.Asp359Gly",
          "transcript": "ENST00000867442.1",
          "protein_id": "ENSP00000537501.1",
          "transcript_support_level": null,
          "aa_start": 359,
          "aa_end": null,
          "aa_length": 431,
          "cds_start": 1076,
          "cds_end": null,
          "cds_length": 1296,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000867442.1"
        },
        {
          "aa_ref": "D",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "GFAP",
          "gene_hgnc_id": 4235,
          "hgvs_c": "c.1079A>G",
          "hgvs_p": "p.Asp360Gly",
          "transcript": "ENST00000867445.1",
          "protein_id": "ENSP00000537504.1",
          "transcript_support_level": null,
          "aa_start": 360,
          "aa_end": null,
          "aa_length": 429,
          "cds_start": 1079,
          "cds_end": null,
          "cds_length": 1290,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000867445.1"
        },
        {
          "aa_ref": "D",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "GFAP",
          "gene_hgnc_id": 4235,
          "hgvs_c": "c.1058A>G",
          "hgvs_p": "p.Asp353Gly",
          "transcript": "ENST00000867444.1",
          "protein_id": "ENSP00000537503.1",
          "transcript_support_level": null,
          "aa_start": 353,
          "aa_end": null,
          "aa_length": 425,
          "cds_start": 1058,
          "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": "ENST00000867444.1"
        },
        {
          "aa_ref": "D",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "GFAP",
          "gene_hgnc_id": 4235,
          "hgvs_c": "c.815A>G",
          "hgvs_p": "p.Asp272Gly",
          "transcript": "ENST00000867446.1",
          "protein_id": "ENSP00000537505.1",
          "transcript_support_level": null,
          "aa_start": 272,
          "aa_end": null,
          "aa_length": 344,
          "cds_start": 815,
          "cds_end": null,
          "cds_length": 1035,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000867446.1"
        },
        {
          "aa_ref": "D",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "GFAP",
          "gene_hgnc_id": 4235,
          "hgvs_c": "c.944A>G",
          "hgvs_p": "p.Asp315Gly",
          "transcript": "ENST00000586793.6",
          "protein_id": "ENSP00000468500.2",
          "transcript_support_level": 5,
          "aa_start": 315,
          "aa_end": null,
          "aa_length": 333,
          "cds_start": 944,
          "cds_end": null,
          "cds_length": 1004,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000586793.6"
        },
        {
          "aa_ref": "D",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "GFAP",
          "gene_hgnc_id": 4235,
          "hgvs_c": "c.734A>G",
          "hgvs_p": "p.Asp245Gly",
          "transcript": "ENST00000638618.1",
          "protein_id": "ENSP00000492832.1",
          "transcript_support_level": 5,
          "aa_start": 245,
          "aa_end": null,
          "aa_length": 326,
          "cds_start": 734,
          "cds_end": null,
          "cds_length": 981,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000638618.1"
        },
        {
          "aa_ref": "D",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "GFAP",
          "gene_hgnc_id": 4235,
          "hgvs_c": "c.656A>G",
          "hgvs_p": "p.Asp219Gly",
          "transcript": "ENST00000592320.6",
          "protein_id": "ENSP00000465320.1",
          "transcript_support_level": 5,
          "aa_start": 219,
          "aa_end": null,
          "aa_length": 247,
          "cds_start": 656,
          "cds_end": null,
          "cds_length": 745,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000592320.6"
        },
        {
          "aa_ref": "D",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "GFAP",
          "gene_hgnc_id": 4235,
          "hgvs_c": "c.14A>G",
          "hgvs_p": "p.Asp5Gly",
          "transcript": "ENST00000586125.2",
          "protein_id": "ENSP00000467397.2",
          "transcript_support_level": 2,
          "aa_start": 5,
          "aa_end": null,
          "aa_length": 124,
          "cds_start": 14,
          "cds_end": null,
          "cds_length": 375,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000586125.2"
        },
        {
          "aa_ref": "D",
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      "acmg_classification": "Pathogenic",
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      "acmg_by_gene": [
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          "verdict": "Pathogenic",
          "transcript": "NM_001363846.2",
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      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
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  ],
  "message": null
}