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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: 16-1819208-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=16&pos=1819208&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "16",
"pos": 1819208,
"ref": "C",
"alt": "T",
"effect": "missense_variant",
"transcript": "NM_005326.6",
"consequences": [
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HAGH",
"gene_hgnc_id": 4805,
"hgvs_c": "c.448G>A",
"hgvs_p": "p.Val150Ile",
"transcript": "NM_005326.6",
"protein_id": "NP_005317.2",
"transcript_support_level": null,
"aa_start": 150,
"aa_end": null,
"aa_length": 308,
"cds_start": 448,
"cds_end": null,
"cds_length": 927,
"cdna_start": 486,
"cdna_end": null,
"cdna_length": 2619,
"mane_select": "ENST00000397356.8",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_005326.6"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HAGH",
"gene_hgnc_id": 4805,
"hgvs_c": "c.448G>A",
"hgvs_p": "p.Val150Ile",
"transcript": "ENST00000397356.8",
"protein_id": "ENSP00000380514.3",
"transcript_support_level": 1,
"aa_start": 150,
"aa_end": null,
"aa_length": 308,
"cds_start": 448,
"cds_end": null,
"cds_length": 927,
"cdna_start": 486,
"cdna_end": null,
"cdna_length": 2619,
"mane_select": "NM_005326.6",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000397356.8"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HAGH",
"gene_hgnc_id": 4805,
"hgvs_c": "n.463G>A",
"hgvs_p": null,
"transcript": "ENST00000569700.5",
"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": 1156,
"mane_select": null,
"mane_plus": null,
"biotype": "retained_intron",
"feature": "ENST00000569700.5"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HAGH",
"gene_hgnc_id": 4805,
"hgvs_c": "c.487G>A",
"hgvs_p": "p.Val163Ile",
"transcript": "ENST00000945501.1",
"protein_id": "ENSP00000615560.1",
"transcript_support_level": null,
"aa_start": 163,
"aa_end": null,
"aa_length": 321,
"cds_start": 487,
"cds_end": null,
"cds_length": 966,
"cdna_start": 536,
"cdna_end": null,
"cdna_length": 1193,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000945501.1"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HAGH",
"gene_hgnc_id": 4805,
"hgvs_c": "c.448G>A",
"hgvs_p": "p.Val150Ile",
"transcript": "ENST00000851988.1",
"protein_id": "ENSP00000522047.1",
"transcript_support_level": null,
"aa_start": 150,
"aa_end": null,
"aa_length": 308,
"cds_start": 448,
"cds_end": null,
"cds_length": 927,
"cdna_start": 463,
"cdna_end": null,
"cdna_length": 1885,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000851988.1"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HAGH",
"gene_hgnc_id": 4805,
"hgvs_c": "c.448G>A",
"hgvs_p": "p.Val150Ile",
"transcript": "ENST00000851989.1",
"protein_id": "ENSP00000522048.1",
"transcript_support_level": null,
"aa_start": 150,
"aa_end": null,
"aa_length": 308,
"cds_start": 448,
"cds_end": null,
"cds_length": 927,
"cdna_start": 488,
"cdna_end": null,
"cdna_length": 2414,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000851989.1"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HAGH",
"gene_hgnc_id": 4805,
"hgvs_c": "c.448G>A",
"hgvs_p": "p.Val150Ile",
"transcript": "ENST00000945502.1",
"protein_id": "ENSP00000615561.1",
"transcript_support_level": null,
"aa_start": 150,
"aa_end": null,
"aa_length": 307,
"cds_start": 448,
"cds_end": null,
"cds_length": 924,
"cdna_start": 492,
"cdna_end": null,
"cdna_length": 1146,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000945502.1"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HAGH",
"gene_hgnc_id": 4805,
"hgvs_c": "c.448G>A",
"hgvs_p": "p.Val150Ile",
"transcript": "NM_001363912.1",
"protein_id": "NP_001350841.1",
"transcript_support_level": null,
"aa_start": 150,
"aa_end": null,
"aa_length": 306,
"cds_start": 448,
"cds_end": null,
"cds_length": 921,
"cdna_start": 855,
"cdna_end": null,
"cdna_length": 1583,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001363912.1"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HAGH",
"gene_hgnc_id": 4805,
"hgvs_c": "c.448G>A",
"hgvs_p": "p.Val150Ile",
"transcript": "ENST00000851990.1",
"protein_id": "ENSP00000522049.1",
"transcript_support_level": null,
"aa_start": 150,
"aa_end": null,
"aa_length": 299,
"cds_start": 448,
"cds_end": null,
"cds_length": 900,
"cdna_start": 486,
"cdna_end": null,
"cdna_length": 1116,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000851990.1"
},
{
"aa_ref": "V",
"aa_alt": "I",
"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": "HAGH",
"gene_hgnc_id": 4805,
"hgvs_c": "c.304G>A",
"hgvs_p": "p.Val102Ile",
"transcript": "NM_001040427.2",
"protein_id": "NP_001035517.1",
"transcript_support_level": null,
"aa_start": 102,
"aa_end": null,
"aa_length": 260,
"cds_start": 304,
"cds_end": null,
"cds_length": 783,
"cdna_start": 951,
"cdna_end": null,
"cdna_length": 1615,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001040427.2"
},
{
"aa_ref": "V",
"aa_alt": "I",
"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": "HAGH",
"gene_hgnc_id": 4805,
"hgvs_c": "c.304G>A",
"hgvs_p": "p.Val102Ile",
"transcript": "ENST00000397353.6",
"protein_id": "ENSP00000380511.2",
"transcript_support_level": 5,
"aa_start": 102,
"aa_end": null,
"aa_length": 260,
"cds_start": 304,
"cds_end": null,
"cds_length": 783,
"cdna_start": 598,
"cdna_end": null,
"cdna_length": 1257,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000397353.6"
},
{
"aa_ref": "V",
"aa_alt": "I",
"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": "HAGH",
"gene_hgnc_id": 4805,
"hgvs_c": "c.304G>A",
"hgvs_p": "p.Val102Ile",
"transcript": "NM_001363914.1",
"protein_id": "NP_001350843.1",
"transcript_support_level": null,
"aa_start": 102,
"aa_end": null,
"aa_length": 258,
"cds_start": 304,
"cds_end": null,
"cds_length": 777,
"cdna_start": 951,
"cdna_end": null,
"cdna_length": 1679,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001363914.1"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HAGH",
"gene_hgnc_id": 4805,
"hgvs_c": "c.304G>A",
"hgvs_p": "p.Val102Ile",
"transcript": "ENST00000566709.5",
"protein_id": "ENSP00000455422.1",
"transcript_support_level": 5,
"aa_start": 102,
"aa_end": null,
"aa_length": 258,
"cds_start": 304,
"cds_end": null,
"cds_length": 777,
"cdna_start": 589,
"cdna_end": null,
"cdna_length": 1291,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000566709.5"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HAGH",
"gene_hgnc_id": 4805,
"hgvs_c": "c.238G>A",
"hgvs_p": "p.Val80Ile",
"transcript": "ENST00000564445.5",
"protein_id": "ENSP00000455355.1",
"transcript_support_level": 3,
"aa_start": 80,
"aa_end": null,
"aa_length": 238,
"cds_start": 238,
"cds_end": null,
"cds_length": 717,
"cdna_start": 239,
"cdna_end": null,
"cdna_length": 864,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000564445.5"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HAGH",
"gene_hgnc_id": 4805,
"hgvs_c": "c.304G>A",
"hgvs_p": "p.Val102Ile",
"transcript": "ENST00000569339.1",
"protein_id": "ENSP00000455970.1",
"transcript_support_level": 3,
"aa_start": 102,
"aa_end": null,
"aa_length": 159,
"cds_start": 304,
"cds_end": null,
"cds_length": 480,
"cdna_start": 644,
"cdna_end": null,
"cdna_length": 820,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000569339.1"
},
{
"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": 7,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "HAGH",
"gene_hgnc_id": 4805,
"hgvs_c": "c.432+689G>A",
"hgvs_p": null,
"transcript": "ENST00000945503.1",
"protein_id": "ENSP00000615562.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 237,
"cds_start": null,
"cds_end": null,
"cds_length": 714,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 908,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000945503.1"
},
{
"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": 8,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "HAGH",
"gene_hgnc_id": 4805,
"hgvs_c": "c.432+689G>A",
"hgvs_p": null,
"transcript": "NM_001286249.2",
"protein_id": "NP_001273178.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 236,
"cds_start": null,
"cds_end": null,
"cds_length": 711,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 1410,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001286249.2"
},
{
"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": 8,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "HAGH",
"gene_hgnc_id": 4805,
"hgvs_c": "c.432+689G>A",
"hgvs_p": null,
"transcript": "ENST00000455446.6",
"protein_id": "ENSP00000406552.2",
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": 236,
"cds_start": null,
"cds_end": null,
"cds_length": 711,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 1276,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000455446.6"
},
{
"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": 8,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "HAGH",
"gene_hgnc_id": 4805,
"hgvs_c": "c.432+689G>A",
"hgvs_p": null,
"transcript": "XM_011522470.4",
"protein_id": "XP_011520772.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 236,
"cds_start": null,
"cds_end": null,
"cds_length": 711,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 1474,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011522470.4"
}
],
"gene_symbol": "HAGH",
"gene_hgnc_id": 4805,
"dbsnp": "rs200922408",
"frequency_reference_population": 0.0000068347435,
"hom_count_reference_population": 0,
"allele_count_reference_population": 11,
"gnomad_exomes_af": 0.00000548975,
"gnomad_genomes_af": 0.0000197156,
"gnomad_exomes_ac": 8,
"gnomad_genomes_ac": 3,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.16993317008018494,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0.029999999329447746,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.24,
"revel_prediction": "Benign",
"alphamissense_score": 0.0857,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.18,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 1.17,
"phylop100way_prediction": "Benign",
"spliceai_max_score": 0.03,
"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": 0,
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "PM2,BP4_Moderate",
"acmg_by_gene": [
{
"score": 0,
"benign_score": 2,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4_Moderate"
],
"verdict": "Uncertain_significance",
"transcript": "NM_005326.6",
"gene_symbol": "HAGH",
"hgnc_id": 4805,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.448G>A",
"hgvs_p": "p.Val150Ile"
}
],
"clinvar_disease": "not specified",
"clinvar_classification": "Uncertain significance",
"clinvar_review_status": "criteria provided, single submitter",
"clinvar_submissions_summary": "US:1",
"phenotype_combined": "not specified",
"pathogenicity_classification_combined": "Uncertain significance",
"custom_annotations": null
}
],
"message": null
}