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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: 20-34725762-T-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=20&pos=34725762&ref=T&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "20",
"pos": 34725762,
"ref": "T",
"alt": "C",
"effect": "intron_variant",
"transcript": "NM_014071.5",
"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": 15,
"intron_rank": 14,
"intron_rank_end": null,
"gene_symbol": "NCOA6",
"gene_hgnc_id": 15936,
"hgvs_c": "c.6148+1497A>G",
"hgvs_p": null,
"transcript": "NM_014071.5",
"protein_id": "NP_054790.2",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 2063,
"cds_start": null,
"cds_end": null,
"cds_length": 6192,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 7083,
"mane_select": "ENST00000359003.7",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_014071.5"
},
{
"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": 15,
"intron_rank": 14,
"intron_rank_end": null,
"gene_symbol": "NCOA6",
"gene_hgnc_id": 15936,
"hgvs_c": "c.6148+1497A>G",
"hgvs_p": null,
"transcript": "ENST00000359003.7",
"protein_id": "ENSP00000351894.2",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 2063,
"cds_start": null,
"cds_end": null,
"cds_length": 6192,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 7083,
"mane_select": "NM_014071.5",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000359003.7"
},
{
"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": 15,
"intron_rank_end": null,
"gene_symbol": "NCOA6",
"gene_hgnc_id": 15936,
"hgvs_c": "c.6148+1497A>G",
"hgvs_p": null,
"transcript": "ENST00000374796.6",
"protein_id": "ENSP00000363929.2",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 2063,
"cds_start": null,
"cds_end": null,
"cds_length": 6192,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 9311,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000374796.6"
},
{
"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": 15,
"intron_rank": 14,
"intron_rank_end": null,
"gene_symbol": "NCOA6",
"gene_hgnc_id": 15936,
"hgvs_c": "c.6163+1497A>G",
"hgvs_p": null,
"transcript": "ENST00000931656.1",
"protein_id": "ENSP00000601715.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 2068,
"cds_start": null,
"cds_end": null,
"cds_length": 6207,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 6989,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000931656.1"
},
{
"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": 15,
"intron_rank": 14,
"intron_rank_end": null,
"gene_symbol": "NCOA6",
"gene_hgnc_id": 15936,
"hgvs_c": "c.6160+1497A>G",
"hgvs_p": null,
"transcript": "ENST00000931655.1",
"protein_id": "ENSP00000601714.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 2067,
"cds_start": null,
"cds_end": null,
"cds_length": 6204,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 7010,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000931655.1"
},
{
"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": 16,
"intron_rank": 15,
"intron_rank_end": null,
"gene_symbol": "NCOA6",
"gene_hgnc_id": 15936,
"hgvs_c": "c.6148+1497A>G",
"hgvs_p": null,
"transcript": "NM_001318240.1",
"protein_id": "NP_001305169.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 2063,
"cds_start": null,
"cds_end": null,
"cds_length": 6192,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 9291,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001318240.1"
},
{
"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": 16,
"intron_rank": 15,
"intron_rank_end": null,
"gene_symbol": "NCOA6",
"gene_hgnc_id": 15936,
"hgvs_c": "c.6148+1497A>G",
"hgvs_p": null,
"transcript": "ENST00000887756.1",
"protein_id": "ENSP00000557815.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 2063,
"cds_start": null,
"cds_end": null,
"cds_length": 6192,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 7088,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000887756.1"
},
{
"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": 16,
"intron_rank": 15,
"intron_rank_end": null,
"gene_symbol": "NCOA6",
"gene_hgnc_id": 15936,
"hgvs_c": "c.6148+1497A>G",
"hgvs_p": null,
"transcript": "ENST00000887757.1",
"protein_id": "ENSP00000557816.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 2063,
"cds_start": null,
"cds_end": null,
"cds_length": 6192,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 7090,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000887757.1"
},
{
"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": 14,
"intron_rank": 13,
"intron_rank_end": null,
"gene_symbol": "NCOA6",
"gene_hgnc_id": 15936,
"hgvs_c": "c.6148+1497A>G",
"hgvs_p": null,
"transcript": "ENST00000931654.1",
"protein_id": "ENSP00000601713.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 2063,
"cds_start": null,
"cds_end": null,
"cds_length": 6192,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 6894,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000931654.1"
},
{
"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": 15,
"intron_rank": 14,
"intron_rank_end": null,
"gene_symbol": "NCOA6",
"gene_hgnc_id": 15936,
"hgvs_c": "c.6145+1497A>G",
"hgvs_p": null,
"transcript": "NM_001438233.1",
"protein_id": "NP_001425162.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 2062,
"cds_start": null,
"cds_end": null,
"cds_length": 6189,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 7080,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001438233.1"
},
{
"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": 15,
"intron_rank": 14,
"intron_rank_end": null,
"gene_symbol": "NCOA6",
"gene_hgnc_id": 15936,
"hgvs_c": "c.6145+1497A>G",
"hgvs_p": null,
"transcript": "ENST00000931651.1",
"protein_id": "ENSP00000601710.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 2062,
"cds_start": null,
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"cds_length": 6189,
"cdna_start": null,
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"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000931651.1"
},
{
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"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"exon_count": 15,
"intron_rank": 14,
"intron_rank_end": null,
"gene_symbol": "NCOA6",
"gene_hgnc_id": 15936,
"hgvs_c": "c.6115+1497A>G",
"hgvs_p": null,
"transcript": "NM_001438235.1",
"protein_id": "NP_001425164.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 2052,
"cds_start": null,
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"cds_length": 6159,
"cdna_start": null,
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"cdna_length": 7050,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001438235.1"
},
{
"aa_ref": null,
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"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": 14,
"intron_rank_end": null,
"gene_symbol": "NCOA6",
"gene_hgnc_id": 15936,
"hgvs_c": "c.6115+1497A>G",
"hgvs_p": null,
"transcript": "ENST00000931653.1",
"protein_id": "ENSP00000601712.1",
"transcript_support_level": null,
"aa_start": null,
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"cds_start": null,
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"cdna_start": null,
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"mane_select": null,
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"biotype": "protein_coding",
"feature": "ENST00000931653.1"
},
{
"aa_ref": null,
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"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"exon_count": 15,
"intron_rank": 14,
"intron_rank_end": null,
"gene_symbol": "NCOA6",
"gene_hgnc_id": 15936,
"hgvs_c": "c.6112+1497A>G",
"hgvs_p": null,
"transcript": "NM_001438234.1",
"protein_id": "NP_001425163.1",
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"mane_select": null,
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"biotype": "protein_coding",
"feature": "NM_001438234.1"
},
{
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"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": 14,
"intron_rank_end": null,
"gene_symbol": "NCOA6",
"gene_hgnc_id": 15936,
"hgvs_c": "c.6112+1497A>G",
"hgvs_p": null,
"transcript": "ENST00000931652.1",
"protein_id": "ENSP00000601711.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
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"cds_start": null,
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"cdna_start": null,
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"mane_select": null,
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"biotype": "protein_coding",
"feature": "ENST00000931652.1"
},
{
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"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"exon_count": 14,
"intron_rank": 13,
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"gene_symbol": "NCOA6",
"gene_hgnc_id": 15936,
"hgvs_c": "c.3169+1497A>G",
"hgvs_p": null,
"transcript": "NM_001242539.3",
"protein_id": "NP_001229468.1",
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"cdna_start": null,
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"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001242539.3"
},
{
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"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": 13,
"intron_rank_end": null,
"gene_symbol": "NCOA6",
"gene_hgnc_id": 15936,
"hgvs_c": "c.3169+1497A>G",
"hgvs_p": null,
"transcript": "ENST00000612493.4",
"protein_id": "ENSP00000481177.1",
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": 1070,
"cds_start": null,
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"cdna_start": null,
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"cdna_length": 4082,
"mane_select": null,
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"biotype": "protein_coding",
"feature": "ENST00000612493.4"
},
{
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"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": 13,
"intron_rank_end": null,
"gene_symbol": "NCOA6",
"gene_hgnc_id": 15936,
"hgvs_c": "c.3133+1497A>G",
"hgvs_p": null,
"transcript": "ENST00000887755.1",
"protein_id": "ENSP00000557814.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
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"cds_start": null,
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"cdna_start": null,
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"mane_select": null,
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"biotype": "protein_coding",
"feature": "ENST00000887755.1"
},
{
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"protein_coding": true,
"strand": false,
"consequences": [
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],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": 5,
"intron_rank_end": null,
"gene_symbol": "NCOA6",
"gene_hgnc_id": 15936,
"hgvs_c": "c.556+1497A>G",
"hgvs_p": null,
"transcript": "ENST00000628752.2",
"protein_id": "ENSP00000486894.1",
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"mane_select": null,
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"biotype": "protein_coding",
"feature": "ENST00000628752.2"
},
{
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"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"exon_count": 16,
"intron_rank": 15,
"intron_rank_end": null,
"gene_symbol": "NCOA6",
"gene_hgnc_id": 15936,
"hgvs_c": "c.6220+1497A>G",
"hgvs_p": null,
"transcript": "XM_017027739.2",
"protein_id": "XP_016883228.1",
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"biotype": "protein_coding",
"feature": "XM_017027739.2"
},
{
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"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": 16,
"intron_rank_end": null,
"gene_symbol": "NCOA6",
"gene_hgnc_id": 15936,
"hgvs_c": "c.6220+1497A>G",
"hgvs_p": null,
"transcript": "XM_047440047.1",
"protein_id": "XP_047296003.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
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"cds_start": null,
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"cdna_start": null,
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"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047440047.1"
},
{
"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": 16,
"intron_rank": 15,
"intron_rank_end": null,
"gene_symbol": "NCOA6",
"gene_hgnc_id": 15936,
"hgvs_c": "c.6217+1497A>G",
"hgvs_p": null,
"transcript": "XM_017027741.2",
"protein_id": "XP_016883230.1",
"transcript_support_level": null,
"aa_start": null,
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"aa_length": 2086,
"cds_start": null,
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"cds_length": 6261,
"cdna_start": null,
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"cdna_length": 7152,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017027741.2"
},
{
"aa_ref": null,
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"splice_prediction_selected": "Benign",
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{
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],
"clinvar_disease": "",
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"custom_annotations": null
}
],
"message": null
}