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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: 16-15667319-C-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=16&pos=15667319&ref=C&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "16",
"pos": 15667319,
"ref": "C",
"alt": "A",
"effect": "missense_variant",
"transcript": "ENST00000396354.6",
"consequences": [
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDE1",
"gene_hgnc_id": 17619,
"hgvs_c": "c.117C>A",
"hgvs_p": "p.Phe39Leu",
"transcript": "NM_017668.3",
"protein_id": "NP_060138.1",
"transcript_support_level": null,
"aa_start": 39,
"aa_end": null,
"aa_length": 335,
"cds_start": 117,
"cds_end": null,
"cds_length": 1008,
"cdna_start": 210,
"cdna_end": null,
"cdna_length": 3203,
"mane_select": "ENST00000396354.6",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDE1",
"gene_hgnc_id": 17619,
"hgvs_c": "c.117C>A",
"hgvs_p": "p.Phe39Leu",
"transcript": "ENST00000396354.6",
"protein_id": "ENSP00000379642.1",
"transcript_support_level": 1,
"aa_start": 39,
"aa_end": null,
"aa_length": 335,
"cds_start": 117,
"cds_end": null,
"cds_length": 1008,
"cdna_start": 210,
"cdna_end": null,
"cdna_length": 3203,
"mane_select": "NM_017668.3",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDE1",
"gene_hgnc_id": 17619,
"hgvs_c": "c.117C>A",
"hgvs_p": "p.Phe39Leu",
"transcript": "ENST00000396355.5",
"protein_id": "ENSP00000379643.1",
"transcript_support_level": 1,
"aa_start": 39,
"aa_end": null,
"aa_length": 335,
"cds_start": 117,
"cds_end": null,
"cds_length": 1008,
"cdna_start": 943,
"cdna_end": null,
"cdna_length": 3936,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDE1",
"gene_hgnc_id": 17619,
"hgvs_c": "c.117C>A",
"hgvs_p": "p.Phe39Leu",
"transcript": "ENST00000577101.6",
"protein_id": "ENSP00000461729.2",
"transcript_support_level": 4,
"aa_start": 39,
"aa_end": null,
"aa_length": 384,
"cds_start": 117,
"cds_end": null,
"cds_length": 1155,
"cdna_start": 117,
"cdna_end": null,
"cdna_length": 3193,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDE1",
"gene_hgnc_id": 17619,
"hgvs_c": "c.117C>A",
"hgvs_p": "p.Phe39Leu",
"transcript": "NM_001143979.2",
"protein_id": "NP_001137451.1",
"transcript_support_level": null,
"aa_start": 39,
"aa_end": null,
"aa_length": 335,
"cds_start": 117,
"cds_end": null,
"cds_length": 1008,
"cdna_start": 828,
"cdna_end": null,
"cdna_length": 3821,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDE1",
"gene_hgnc_id": 17619,
"hgvs_c": "c.117C>A",
"hgvs_p": "p.Phe39Leu",
"transcript": "ENST00000674995.1",
"protein_id": "ENSP00000502414.1",
"transcript_support_level": null,
"aa_start": 39,
"aa_end": null,
"aa_length": 317,
"cds_start": 117,
"cds_end": null,
"cds_length": 954,
"cdna_start": 192,
"cdna_end": null,
"cdna_length": 5636,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDE1",
"gene_hgnc_id": 17619,
"hgvs_c": "c.117C>A",
"hgvs_p": "p.Phe39Leu",
"transcript": "ENST00000572756.6",
"protein_id": "ENSP00000460436.2",
"transcript_support_level": 5,
"aa_start": 39,
"aa_end": null,
"aa_length": 283,
"cds_start": 117,
"cds_end": null,
"cds_length": 853,
"cdna_start": 117,
"cdna_end": null,
"cdna_length": 853,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDE1",
"gene_hgnc_id": 17619,
"hgvs_c": "c.117C>A",
"hgvs_p": "p.Phe39Leu",
"transcript": "ENST00000674581.1",
"protein_id": "ENSP00000502100.1",
"transcript_support_level": null,
"aa_start": 39,
"aa_end": null,
"aa_length": 282,
"cds_start": 117,
"cds_end": null,
"cds_length": 849,
"cdna_start": 192,
"cdna_end": null,
"cdna_length": 3093,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDE1",
"gene_hgnc_id": 17619,
"hgvs_c": "c.117C>A",
"hgvs_p": "p.Phe39Leu",
"transcript": "ENST00000570727.5",
"protein_id": "ENSP00000459889.1",
"transcript_support_level": 4,
"aa_start": 39,
"aa_end": null,
"aa_length": 126,
"cds_start": 117,
"cds_end": null,
"cds_length": 381,
"cdna_start": 324,
"cdna_end": null,
"cdna_length": 588,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDE1",
"gene_hgnc_id": 17619,
"hgvs_c": "c.213C>A",
"hgvs_p": "p.Phe71Leu",
"transcript": "XM_006720897.5",
"protein_id": "XP_006720960.1",
"transcript_support_level": null,
"aa_start": 71,
"aa_end": null,
"aa_length": 379,
"cds_start": 213,
"cds_end": null,
"cds_length": 1140,
"cdna_start": 706,
"cdna_end": null,
"cdna_length": 1795,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDE1",
"gene_hgnc_id": 17619,
"hgvs_c": "c.213C>A",
"hgvs_p": "p.Phe71Leu",
"transcript": "XM_047434258.1",
"protein_id": "XP_047290214.1",
"transcript_support_level": null,
"aa_start": 71,
"aa_end": null,
"aa_length": 378,
"cds_start": 213,
"cds_end": null,
"cds_length": 1137,
"cdna_start": 706,
"cdna_end": null,
"cdna_length": 1795,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDE1",
"gene_hgnc_id": 17619,
"hgvs_c": "c.213C>A",
"hgvs_p": "p.Phe71Leu",
"transcript": "XM_047434259.1",
"protein_id": "XP_047290215.1",
"transcript_support_level": null,
"aa_start": 71,
"aa_end": null,
"aa_length": 377,
"cds_start": 213,
"cds_end": null,
"cds_length": 1134,
"cdna_start": 706,
"cdna_end": null,
"cdna_length": 3719,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDE1",
"gene_hgnc_id": 17619,
"hgvs_c": "c.213C>A",
"hgvs_p": "p.Phe71Leu",
"transcript": "XM_047434260.1",
"protein_id": "XP_047290216.1",
"transcript_support_level": null,
"aa_start": 71,
"aa_end": null,
"aa_length": 371,
"cds_start": 213,
"cds_end": null,
"cds_length": 1116,
"cdna_start": 706,
"cdna_end": null,
"cdna_length": 1704,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDE1",
"gene_hgnc_id": 17619,
"hgvs_c": "c.213C>A",
"hgvs_p": "p.Phe71Leu",
"transcript": "XM_047434261.1",
"protein_id": "XP_047290217.1",
"transcript_support_level": null,
"aa_start": 71,
"aa_end": null,
"aa_length": 351,
"cds_start": 213,
"cds_end": null,
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"cdna_start": 706,
"cdna_end": null,
"cdna_length": 3570,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDE1",
"gene_hgnc_id": 17619,
"hgvs_c": "c.117C>A",
"hgvs_p": "p.Phe39Leu",
"transcript": "XM_005255396.6",
"protein_id": "XP_005255453.1",
"transcript_support_level": null,
"aa_start": 39,
"aa_end": null,
"aa_length": 347,
"cds_start": 117,
"cds_end": null,
"cds_length": 1044,
"cdna_start": 210,
"cdna_end": null,
"cdna_length": 1299,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDE1",
"gene_hgnc_id": 17619,
"hgvs_c": "c.117C>A",
"hgvs_p": "p.Phe39Leu",
"transcript": "XM_006720900.5",
"protein_id": "XP_006720963.1",
"transcript_support_level": null,
"aa_start": 39,
"aa_end": null,
"aa_length": 347,
"cds_start": 117,
"cds_end": null,
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"cdna_start": 195,
"cdna_end": null,
"cdna_length": 1284,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDE1",
"gene_hgnc_id": 17619,
"hgvs_c": "c.117C>A",
"hgvs_p": "p.Phe39Leu",
"transcript": "XM_047434262.1",
"protein_id": "XP_047290218.1",
"transcript_support_level": null,
"aa_start": 39,
"aa_end": null,
"aa_length": 347,
"cds_start": 117,
"cds_end": null,
"cds_length": 1044,
"cdna_start": 183,
"cdna_end": null,
"cdna_length": 1272,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDE1",
"gene_hgnc_id": 17619,
"hgvs_c": "c.117C>A",
"hgvs_p": "p.Phe39Leu",
"transcript": "XM_017023349.3",
"protein_id": "XP_016878838.1",
"transcript_support_level": null,
"aa_start": 39,
"aa_end": null,
"aa_length": 346,
"cds_start": 117,
"cds_end": null,
"cds_length": 1041,
"cdna_start": 210,
"cdna_end": null,
"cdna_length": 3226,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDE1",
"gene_hgnc_id": 17619,
"hgvs_c": "c.117C>A",
"hgvs_p": "p.Phe39Leu",
"transcript": "XM_017023350.2",
"protein_id": "XP_016878839.1",
"transcript_support_level": null,
"aa_start": 39,
"aa_end": null,
"aa_length": 346,
"cds_start": 117,
"cds_end": null,
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"cdna_start": 210,
"cdna_end": null,
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"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDE1",
"gene_hgnc_id": 17619,
"hgvs_c": "c.117C>A",
"hgvs_p": "p.Phe39Leu",
"transcript": "XM_047434263.1",
"protein_id": "XP_047290219.1",
"transcript_support_level": null,
"aa_start": 39,
"aa_end": null,
"aa_length": 345,
"cds_start": 117,
"cds_end": null,
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"cdna_start": 210,
"cdna_end": null,
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"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDE1",
"gene_hgnc_id": 17619,
"hgvs_c": "c.117C>A",
"hgvs_p": "p.Phe39Leu",
"transcript": "XM_017023352.3",
"protein_id": "XP_016878841.1",
"transcript_support_level": null,
"aa_start": 39,
"aa_end": null,
"aa_length": 339,
"cds_start": 117,
"cds_end": null,
"cds_length": 1020,
"cdna_start": 210,
"cdna_end": null,
"cdna_length": 1208,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDE1",
"gene_hgnc_id": 17619,
"hgvs_c": "c.213C>A",
"hgvs_p": "p.Phe71Leu",
"transcript": "XM_047434264.1",
"protein_id": "XP_047290220.1",
"transcript_support_level": null,
"aa_start": 71,
"aa_end": null,
"aa_length": 333,
"cds_start": 213,
"cds_end": null,
"cds_length": 1002,
"cdna_start": 706,
"cdna_end": null,
"cdna_length": 1665,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDE1",
"gene_hgnc_id": 17619,
"hgvs_c": "c.117C>A",
"hgvs_p": "p.Phe39Leu",
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