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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: 12-109247740-A-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=12&pos=109247740&ref=A&alt=G&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "12",
"pos": 109247740,
"ref": "A",
"alt": "G",
"effect": "intron_variant",
"transcript": "ENST00000338432.12",
"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": 53,
"intron_rank": 40,
"intron_rank_end": null,
"gene_symbol": "ACACB",
"gene_hgnc_id": 85,
"hgvs_c": "c.5669+37A>G",
"hgvs_p": null,
"transcript": "NM_001093.4",
"protein_id": "NP_001084.3",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 2458,
"cds_start": -4,
"cds_end": null,
"cds_length": 7377,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 9368,
"mane_select": "ENST00000338432.12",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 53,
"intron_rank": 40,
"intron_rank_end": null,
"gene_symbol": "ACACB",
"gene_hgnc_id": 85,
"hgvs_c": "c.5669+37A>G",
"hgvs_p": null,
"transcript": "ENST00000338432.12",
"protein_id": "ENSP00000341044.7",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 2458,
"cds_start": -4,
"cds_end": null,
"cds_length": 7377,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 9368,
"mane_select": "NM_001093.4",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 52,
"intron_rank": 39,
"intron_rank_end": null,
"gene_symbol": "ACACB",
"gene_hgnc_id": 85,
"hgvs_c": "c.5669+37A>G",
"hgvs_p": null,
"transcript": "ENST00000377848.7",
"protein_id": "ENSP00000367079.3",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 2458,
"cds_start": -4,
"cds_end": null,
"cds_length": 7377,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 9247,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 54,
"intron_rank": 41,
"intron_rank_end": null,
"gene_symbol": "ACACB",
"gene_hgnc_id": 85,
"hgvs_c": "c.5669+37A>G",
"hgvs_p": null,
"transcript": "NM_001412734.1",
"protein_id": "NP_001399663.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 2458,
"cds_start": -4,
"cds_end": null,
"cds_length": 7377,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 9855,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 53,
"intron_rank": 40,
"intron_rank_end": null,
"gene_symbol": "ACACB",
"gene_hgnc_id": 85,
"hgvs_c": "c.5669+37A>G",
"hgvs_p": null,
"transcript": "NM_001412735.1",
"protein_id": "NP_001399664.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 2458,
"cds_start": -4,
"cds_end": null,
"cds_length": 7377,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 9316,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 52,
"intron_rank": 39,
"intron_rank_end": null,
"gene_symbol": "ACACB",
"gene_hgnc_id": 85,
"hgvs_c": "c.5063+37A>G",
"hgvs_p": null,
"transcript": "NM_001412736.1",
"protein_id": "NP_001399665.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 2256,
"cds_start": -4,
"cds_end": null,
"cds_length": 6771,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 8850,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 53,
"intron_rank": 40,
"intron_rank_end": null,
"gene_symbol": "ACACB",
"gene_hgnc_id": 85,
"hgvs_c": "c.5042+37A>G",
"hgvs_p": null,
"transcript": "NM_001412737.1",
"protein_id": "NP_001399666.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 2249,
"cds_start": -4,
"cds_end": null,
"cds_length": 6750,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 9027,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 51,
"intron_rank": 38,
"intron_rank_end": null,
"gene_symbol": "ACACB",
"gene_hgnc_id": 85,
"hgvs_c": "c.4874+37A>G",
"hgvs_p": null,
"transcript": "NM_001412738.1",
"protein_id": "NP_001399667.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 2193,
"cds_start": -4,
"cds_end": null,
"cds_length": 6582,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 8661,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 41,
"intron_rank": 39,
"intron_rank_end": null,
"gene_symbol": "ACACB",
"gene_hgnc_id": 85,
"hgvs_c": "c.5063+37A>G",
"hgvs_p": null,
"transcript": "NM_001412739.1",
"protein_id": "NP_001399668.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1819,
"cds_start": -4,
"cds_end": null,
"cds_length": 5460,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 5932,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 47,
"intron_rank": 39,
"intron_rank_end": null,
"gene_symbol": "ACACB",
"gene_hgnc_id": 85,
"hgvs_c": "c.1667+37A>G",
"hgvs_p": null,
"transcript": "ENST00000377854.9",
"protein_id": "ENSP00000367085.6",
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": 858,
"cds_start": -4,
"cds_end": null,
"cds_length": 2577,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 6588,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
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"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "ACACB",
"gene_hgnc_id": 85,
"hgvs_c": "n.303+1292A>G",
"hgvs_p": null,
"transcript": "ENST00000536440.2",
"protein_id": "ENSP00000478488.1",
"transcript_support_level": 3,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
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"feature": null
},
{
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"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"exon_count": 26,
"intron_rank": 12,
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"gene_symbol": "ACACB",
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"hgvs_c": "n.1667+37A>G",
"hgvs_p": null,
"transcript": "ENST00000538526.5",
"protein_id": "ENSP00000443281.1",
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"cds_start": -4,
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"cdna_start": null,
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"cdna_length": 3654,
"mane_select": null,
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"feature": null
},
{
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"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 52,
"intron_rank": 39,
"intron_rank_end": null,
"gene_symbol": "ACACB",
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"hgvs_c": "c.5480+37A>G",
"hgvs_p": null,
"transcript": "XM_011538263.4",
"protein_id": "XP_011536565.1",
"transcript_support_level": null,
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},
{
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"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"exon_count": 52,
"intron_rank": 39,
"intron_rank_end": null,
"gene_symbol": "ACACB",
"gene_hgnc_id": 85,
"hgvs_c": "c.5042+37A>G",
"hgvs_p": null,
"transcript": "XM_011538264.4",
"protein_id": "XP_011536566.1",
"transcript_support_level": null,
"aa_start": null,
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"feature": null
},
{
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"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"intron_rank": 40,
"intron_rank_end": null,
"gene_symbol": "ACACB",
"gene_hgnc_id": 85,
"hgvs_c": "c.5042+37A>G",
"hgvs_p": null,
"transcript": "XM_047428764.1",
"protein_id": "XP_047284720.1",
"transcript_support_level": null,
"aa_start": null,
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"cds_start": -4,
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"mane_select": null,
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"biotype": null,
"feature": null
},
{
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"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 52,
"intron_rank": 39,
"intron_rank_end": null,
"gene_symbol": "ACACB",
"gene_hgnc_id": 85,
"hgvs_c": "c.5009+37A>G",
"hgvs_p": null,
"transcript": "XM_047428765.1",
"protein_id": "XP_047284721.1",
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},
{
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],
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"gene_symbol": "ACACB",
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"hgvs_c": "c.5669+37A>G",
"hgvs_p": null,
"transcript": "XM_047428766.1",
"protein_id": "XP_047284722.1",
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},
{
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"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"exon_count": 49,
"intron_rank": 40,
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"gene_symbol": "ACACB",
"gene_hgnc_id": 85,
"hgvs_c": "c.5669+37A>G",
"hgvs_p": null,
"transcript": "XM_047428767.1",
"protein_id": "XP_047284723.1",
"transcript_support_level": null,
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},
{
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"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"exon_count": 48,
"intron_rank": 40,
"intron_rank_end": null,
"gene_symbol": "ACACB",
"gene_hgnc_id": 85,
"hgvs_c": "c.5669+37A>G",
"hgvs_p": null,
"transcript": "XM_047428768.1",
"protein_id": "XP_047284724.1",
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},
{
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"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"exon_count": 41,
"intron_rank": 39,
"intron_rank_end": null,
"gene_symbol": "ACACB",
"gene_hgnc_id": 85,
"hgvs_c": "n.7419+1292A>G",
"hgvs_p": null,
"transcript": "XR_007063072.1",
"protein_id": null,
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"feature": null
}
],
"gene_symbol": "ACACB",
"gene_hgnc_id": 85,
"dbsnp": "rs2284689",
"frequency_reference_population": 0.8029178,
"hom_count_reference_population": 495798,
"allele_count_reference_population": 1229569,
"gnomad_exomes_af": 0.806009,
"gnomad_genomes_af": 0.774879,
"gnomad_exomes_ac": 1111727,
"gnomad_genomes_ac": 117842,
"gnomad_exomes_homalt": 449647,
"gnomad_genomes_homalt": 46151,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": -0.8999999761581421,
"computational_prediction_selected": "Benign",
"computational_source_selected": "BayesDel_noAF",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": null,
"revel_prediction": null,
"alphamissense_score": null,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.9,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": -1.09,
"phylop100way_prediction": "Benign",
"spliceai_max_score": 0,
"spliceai_max_prediction": "Benign",
"dbscsnv_ada_score": null,
"dbscsnv_ada_prediction": null,
"apogee2_score": null,
"apogee2_prediction": null,
"mitotip_score": null,
"mitotip_prediction": null,
"acmg_score": -12,
"acmg_classification": "Benign",
"acmg_criteria": "BP4_Strong,BA1",
"acmg_by_gene": [
{
"score": -12,
"benign_score": 12,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong",
"BA1"
],
"verdict": "Benign",
"transcript": "ENST00000338432.12",
"gene_symbol": "ACACB",
"hgnc_id": 85,
"effects": [
"intron_variant"
],
"inheritance_mode": "Unknown",
"hgvs_c": "c.5669+37A>G",
"hgvs_p": null
}
],
"clinvar_disease": "",
"clinvar_classification": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"phenotype_combined": null,
"pathogenicity_classification_combined": null,
"custom_annotations": null
}
],
"message": null
}