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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: 9-16419027-T-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=9&pos=16419027&ref=T&alt=G&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "9",
"pos": 16419027,
"ref": "T",
"alt": "G",
"effect": "missense_variant",
"transcript": "NM_017637.6",
"consequences": [
{
"aa_ref": "N",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BNC2",
"gene_hgnc_id": 30988,
"hgvs_c": "c.3262A>C",
"hgvs_p": "p.Asn1088His",
"transcript": "NM_017637.6",
"protein_id": "NP_060107.3",
"transcript_support_level": null,
"aa_start": 1088,
"aa_end": null,
"aa_length": 1099,
"cds_start": 3262,
"cds_end": null,
"cds_length": 3300,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000380672.9",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_017637.6"
},
{
"aa_ref": "N",
"aa_alt": "H",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BNC2",
"gene_hgnc_id": 30988,
"hgvs_c": "c.3262A>C",
"hgvs_p": "p.Asn1088His",
"transcript": "ENST00000380672.9",
"protein_id": "ENSP00000370047.3",
"transcript_support_level": 2,
"aa_start": 1088,
"aa_end": null,
"aa_length": 1099,
"cds_start": 3262,
"cds_end": null,
"cds_length": 3300,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_017637.6",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000380672.9"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BNC2",
"gene_hgnc_id": 30988,
"hgvs_c": "c.*606A>C",
"hgvs_p": null,
"transcript": "ENST00000545497.5",
"protein_id": "ENSP00000444640.2",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 729,
"cds_start": null,
"cds_end": null,
"cds_length": 2190,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000545497.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BNC2",
"gene_hgnc_id": 30988,
"hgvs_c": "c.*638A>C",
"hgvs_p": null,
"transcript": "ENST00000411752.5",
"protein_id": "ENSP00000392212.1",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 327,
"cds_start": null,
"cds_end": null,
"cds_length": 984,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000411752.5"
},
{
"aa_ref": "N",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BNC2",
"gene_hgnc_id": 30988,
"hgvs_c": "c.3373A>C",
"hgvs_p": "p.Asn1125His",
"transcript": "ENST00000863292.1",
"protein_id": "ENSP00000533351.1",
"transcript_support_level": null,
"aa_start": 1125,
"aa_end": null,
"aa_length": 1136,
"cds_start": 3373,
"cds_end": null,
"cds_length": 3411,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000863292.1"
},
{
"aa_ref": "N",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BNC2",
"gene_hgnc_id": 30988,
"hgvs_c": "c.3346A>C",
"hgvs_p": "p.Asn1116His",
"transcript": "ENST00000863291.1",
"protein_id": "ENSP00000533350.1",
"transcript_support_level": null,
"aa_start": 1116,
"aa_end": null,
"aa_length": 1127,
"cds_start": 3346,
"cds_end": null,
"cds_length": 3384,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000863291.1"
},
{
"aa_ref": "N",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BNC2",
"gene_hgnc_id": 30988,
"hgvs_c": "c.3247A>C",
"hgvs_p": "p.Asn1083His",
"transcript": "ENST00000863289.1",
"protein_id": "ENSP00000533348.1",
"transcript_support_level": null,
"aa_start": 1083,
"aa_end": null,
"aa_length": 1094,
"cds_start": 3247,
"cds_end": null,
"cds_length": 3285,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000863289.1"
},
{
"aa_ref": "N",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BNC2",
"gene_hgnc_id": 30988,
"hgvs_c": "c.3220A>C",
"hgvs_p": "p.Asn1074His",
"transcript": "ENST00000928770.1",
"protein_id": "ENSP00000598829.1",
"transcript_support_level": null,
"aa_start": 1074,
"aa_end": null,
"aa_length": 1085,
"cds_start": 3220,
"cds_end": null,
"cds_length": 3258,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000928770.1"
},
{
"aa_ref": "N",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BNC2",
"gene_hgnc_id": 30988,
"hgvs_c": "c.3172A>C",
"hgvs_p": "p.Asn1058His",
"transcript": "ENST00000863290.1",
"protein_id": "ENSP00000533349.1",
"transcript_support_level": null,
"aa_start": 1058,
"aa_end": null,
"aa_length": 1069,
"cds_start": 3172,
"cds_end": null,
"cds_length": 3210,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000863290.1"
},
{
"aa_ref": "N",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BNC2",
"gene_hgnc_id": 30988,
"hgvs_c": "c.3145A>C",
"hgvs_p": "p.Asn1049His",
"transcript": "ENST00000863293.1",
"protein_id": "ENSP00000533352.1",
"transcript_support_level": null,
"aa_start": 1049,
"aa_end": null,
"aa_length": 1060,
"cds_start": 3145,
"cds_end": null,
"cds_length": 3183,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000863293.1"
},
{
"aa_ref": "N",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BNC2",
"gene_hgnc_id": 30988,
"hgvs_c": "c.3061A>C",
"hgvs_p": "p.Asn1021His",
"transcript": "ENST00000380667.6",
"protein_id": "ENSP00000370042.1",
"transcript_support_level": 5,
"aa_start": 1021,
"aa_end": null,
"aa_length": 1032,
"cds_start": 3061,
"cds_end": null,
"cds_length": 3099,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000380667.6"
},
{
"aa_ref": "N",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BNC2",
"gene_hgnc_id": 30988,
"hgvs_c": "c.2998A>C",
"hgvs_p": "p.Asn1000His",
"transcript": "ENST00000700553.1",
"protein_id": "ENSP00000515060.1",
"transcript_support_level": null,
"aa_start": 1000,
"aa_end": null,
"aa_length": 1011,
"cds_start": 2998,
"cds_end": null,
"cds_length": 3036,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000700553.1"
},
{
"aa_ref": "N",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BNC2",
"gene_hgnc_id": 30988,
"hgvs_c": "c.2977A>C",
"hgvs_p": "p.Asn993His",
"transcript": "NM_001317940.2",
"protein_id": "NP_001304869.1",
"transcript_support_level": null,
"aa_start": 993,
"aa_end": null,
"aa_length": 1004,
"cds_start": 2977,
"cds_end": null,
"cds_length": 3015,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001317940.2"
},
{
"aa_ref": "N",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BNC2",
"gene_hgnc_id": 30988,
"hgvs_c": "c.3529A>C",
"hgvs_p": "p.Asn1177His",
"transcript": "XM_047423480.1",
"protein_id": "XP_047279436.1",
"transcript_support_level": null,
"aa_start": 1177,
"aa_end": null,
"aa_length": 1188,
"cds_start": 3529,
"cds_end": null,
"cds_length": 3567,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047423480.1"
},
{
"aa_ref": "N",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BNC2",
"gene_hgnc_id": 30988,
"hgvs_c": "c.3454A>C",
"hgvs_p": "p.Asn1152His",
"transcript": "XM_047423481.1",
"protein_id": "XP_047279437.1",
"transcript_support_level": null,
"aa_start": 1152,
"aa_end": null,
"aa_length": 1163,
"cds_start": 3454,
"cds_end": null,
"cds_length": 3492,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047423481.1"
},
{
"aa_ref": "N",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BNC2",
"gene_hgnc_id": 30988,
"hgvs_c": "c.3445A>C",
"hgvs_p": "p.Asn1149His",
"transcript": "XM_047423482.1",
"protein_id": "XP_047279438.1",
"transcript_support_level": null,
"aa_start": 1149,
"aa_end": null,
"aa_length": 1160,
"cds_start": 3445,
"cds_end": null,
"cds_length": 3483,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047423482.1"
},
{
"aa_ref": "N",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BNC2",
"gene_hgnc_id": 30988,
"hgvs_c": "c.3403A>C",
"hgvs_p": "p.Asn1135His",
"transcript": "XM_047423483.1",
"protein_id": "XP_047279439.1",
"transcript_support_level": null,
"aa_start": 1135,
"aa_end": null,
"aa_length": 1146,
"cds_start": 3403,
"cds_end": null,
"cds_length": 3441,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047423483.1"
},
{
"aa_ref": "N",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BNC2",
"gene_hgnc_id": 30988,
"hgvs_c": "c.3388A>C",
"hgvs_p": "p.Asn1130His",
"transcript": "XM_047423484.1",
"protein_id": "XP_047279440.1",
"transcript_support_level": null,
"aa_start": 1130,
"aa_end": null,
"aa_length": 1141,
"cds_start": 3388,
"cds_end": null,
"cds_length": 3426,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047423484.1"
},
{
"aa_ref": "N",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BNC2",
"gene_hgnc_id": 30988,
"hgvs_c": "c.3382A>C",
"hgvs_p": "p.Asn1128His",
"transcript": "XM_047423485.1",
"protein_id": "XP_047279441.1",
"transcript_support_level": null,
"aa_start": 1128,
"aa_end": null,
"aa_length": 1139,
"cds_start": 3382,
"cds_end": null,
"cds_length": 3420,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047423485.1"
},
{
"aa_ref": "N",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BNC2",
"gene_hgnc_id": 30988,
"hgvs_c": "c.3370A>C",
"hgvs_p": "p.Asn1124His",
"transcript": "XM_047423486.1",
"protein_id": "XP_047279442.1",
"transcript_support_level": null,
"aa_start": 1124,
"aa_end": null,
"aa_length": 1135,
"cds_start": 3370,
"cds_end": null,
"cds_length": 3408,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047423486.1"
},
{
"aa_ref": "N",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BNC2",
"gene_hgnc_id": 30988,
"hgvs_c": "c.3346A>C",
"hgvs_p": "p.Asn1116His",
"transcript": "XM_047423487.1",
"protein_id": "XP_047279443.1",
"transcript_support_level": null,
"aa_start": 1116,
"aa_end": null,
"aa_length": 1127,
"cds_start": 3346,
"cds_end": null,
"cds_length": 3384,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047423487.1"
},
{
"aa_ref": "N",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BNC2",
"gene_hgnc_id": 30988,
"hgvs_c": "c.3328A>C",
"hgvs_p": "p.Asn1110His",
"transcript": "XM_047423488.1",
"protein_id": "XP_047279444.1",
"transcript_support_level": null,
"aa_start": 1110,
"aa_end": null,
"aa_length": 1121,
"cds_start": 3328,
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}
],
"message": null
}