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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: 14-79861690-G-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=14&pos=79861690&ref=G&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "14",
"pos": 79861690,
"ref": "G",
"alt": "C",
"effect": "missense_variant",
"transcript": "NM_001330195.2",
"consequences": [
{
"aa_ref": "R",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NRXN3",
"gene_hgnc_id": 8010,
"hgvs_c": "c.4442G>C",
"hgvs_p": "p.Arg1481Pro",
"transcript": "NM_001330195.2",
"protein_id": "NP_001317124.1",
"transcript_support_level": null,
"aa_start": 1481,
"aa_end": null,
"aa_length": 1571,
"cds_start": 4442,
"cds_end": null,
"cds_length": 4716,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000335750.7",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001330195.2"
},
{
"aa_ref": "R",
"aa_alt": "P",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NRXN3",
"gene_hgnc_id": 8010,
"hgvs_c": "c.4442G>C",
"hgvs_p": "p.Arg1481Pro",
"transcript": "ENST00000335750.7",
"protein_id": "ENSP00000338349.7",
"transcript_support_level": 5,
"aa_start": 1481,
"aa_end": null,
"aa_length": 1571,
"cds_start": 4442,
"cds_end": null,
"cds_length": 4716,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_001330195.2",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000335750.7"
},
{
"aa_ref": "R",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NRXN3",
"gene_hgnc_id": 8010,
"hgvs_c": "c.2912G>C",
"hgvs_p": "p.Arg971Pro",
"transcript": "ENST00000554719.5",
"protein_id": "ENSP00000451648.1",
"transcript_support_level": 1,
"aa_start": 971,
"aa_end": null,
"aa_length": 1061,
"cds_start": 2912,
"cds_end": null,
"cds_length": 3186,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000554719.5"
},
{
"aa_ref": "R",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NRXN3",
"gene_hgnc_id": 8010,
"hgvs_c": "c.1106G>C",
"hgvs_p": "p.Arg369Pro",
"transcript": "ENST00000428277.6",
"protein_id": "ENSP00000394426.2",
"transcript_support_level": 1,
"aa_start": 369,
"aa_end": null,
"aa_length": 459,
"cds_start": 1106,
"cds_end": null,
"cds_length": 1380,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000428277.6"
},
{
"aa_ref": "R",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NRXN3",
"gene_hgnc_id": 8010,
"hgvs_c": "c.1025G>C",
"hgvs_p": "p.Arg342Pro",
"transcript": "ENST00000281127.11",
"protein_id": "ENSP00000281127.7",
"transcript_support_level": 1,
"aa_start": 342,
"aa_end": null,
"aa_length": 432,
"cds_start": 1025,
"cds_end": null,
"cds_length": 1299,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000281127.11"
},
{
"aa_ref": "R",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NRXN3",
"gene_hgnc_id": 8010,
"hgvs_c": "c.4352G>C",
"hgvs_p": "p.Arg1451Pro",
"transcript": "NM_001366425.1",
"protein_id": "NP_001353354.1",
"transcript_support_level": null,
"aa_start": 1451,
"aa_end": null,
"aa_length": 1541,
"cds_start": 4352,
"cds_end": null,
"cds_length": 4626,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001366425.1"
},
{
"aa_ref": "R",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 22,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NRXN3",
"gene_hgnc_id": 8010,
"hgvs_c": "c.4133G>C",
"hgvs_p": "p.Arg1378Pro",
"transcript": "NM_001366426.1",
"protein_id": "NP_001353355.1",
"transcript_support_level": null,
"aa_start": 1378,
"aa_end": null,
"aa_length": 1468,
"cds_start": 4133,
"cds_end": null,
"cds_length": 4407,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001366426.1"
},
{
"aa_ref": "R",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 22,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NRXN3",
"gene_hgnc_id": 8010,
"hgvs_c": "c.4133G>C",
"hgvs_p": "p.Arg1378Pro",
"transcript": "ENST00000634499.2",
"protein_id": "ENSP00000488920.2",
"transcript_support_level": 5,
"aa_start": 1378,
"aa_end": null,
"aa_length": 1468,
"cds_start": 4133,
"cds_end": null,
"cds_length": 4407,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000634499.2"
},
{
"aa_ref": "R",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NRXN3",
"gene_hgnc_id": 8010,
"hgvs_c": "c.3710G>C",
"hgvs_p": "p.Arg1237Pro",
"transcript": "ENST00000635466.2",
"protein_id": "ENSP00000489551.2",
"transcript_support_level": 5,
"aa_start": 1237,
"aa_end": null,
"aa_length": 1327,
"cds_start": 3710,
"cds_end": null,
"cds_length": 3984,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000635466.2"
},
{
"aa_ref": "R",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NRXN3",
"gene_hgnc_id": 8010,
"hgvs_c": "c.2912G>C",
"hgvs_p": "p.Arg971Pro",
"transcript": "NM_004796.6",
"protein_id": "NP_004787.2",
"transcript_support_level": null,
"aa_start": 971,
"aa_end": null,
"aa_length": 1061,
"cds_start": 2912,
"cds_end": null,
"cds_length": 3186,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_004796.6"
},
{
"aa_ref": "R",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NRXN3",
"gene_hgnc_id": 8010,
"hgvs_c": "c.1739G>C",
"hgvs_p": "p.Arg580Pro",
"transcript": "ENST00000679122.1",
"protein_id": "ENSP00000502844.1",
"transcript_support_level": null,
"aa_start": 580,
"aa_end": null,
"aa_length": 670,
"cds_start": 1739,
"cds_end": null,
"cds_length": 2013,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000679122.1"
},
{
"aa_ref": "R",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NRXN3",
"gene_hgnc_id": 8010,
"hgvs_c": "c.1640G>C",
"hgvs_p": "p.Arg547Pro",
"transcript": "NM_001272020.2",
"protein_id": "NP_001258949.1",
"transcript_support_level": null,
"aa_start": 547,
"aa_end": null,
"aa_length": 637,
"cds_start": 1640,
"cds_end": null,
"cds_length": 1914,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001272020.2"
},
{
"aa_ref": "R",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NRXN3",
"gene_hgnc_id": 8010,
"hgvs_c": "c.1640G>C",
"hgvs_p": "p.Arg547Pro",
"transcript": "ENST00000557594.5",
"protein_id": "ENSP00000451672.1",
"transcript_support_level": 2,
"aa_start": 547,
"aa_end": null,
"aa_length": 637,
"cds_start": 1640,
"cds_end": null,
"cds_length": 1914,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000557594.5"
},
{
"aa_ref": "R",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NRXN3",
"gene_hgnc_id": 8010,
"hgvs_c": "c.1106G>C",
"hgvs_p": "p.Arg369Pro",
"transcript": "NM_001105250.3",
"protein_id": "NP_001098720.1",
"transcript_support_level": null,
"aa_start": 369,
"aa_end": null,
"aa_length": 459,
"cds_start": 1106,
"cds_end": null,
"cds_length": 1380,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001105250.3"
},
{
"aa_ref": "R",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NRXN3",
"gene_hgnc_id": 8010,
"hgvs_c": "c.1025G>C",
"hgvs_p": "p.Arg342Pro",
"transcript": "NM_138970.5",
"protein_id": "NP_620426.2",
"transcript_support_level": null,
"aa_start": 342,
"aa_end": null,
"aa_length": 432,
"cds_start": 1025,
"cds_end": null,
"cds_length": 1299,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_138970.5"
},
{
"aa_ref": "R",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 23,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NRXN3",
"gene_hgnc_id": 8010,
"hgvs_c": "c.4790G>C",
"hgvs_p": "p.Arg1597Pro",
"transcript": "XM_011537363.2",
"protein_id": "XP_011535665.1",
"transcript_support_level": null,
"aa_start": 1597,
"aa_end": null,
"aa_length": 1687,
"cds_start": 4790,
"cds_end": null,
"cds_length": 5064,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011537363.2"
},
{
"aa_ref": "R",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 23,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NRXN3",
"gene_hgnc_id": 8010,
"hgvs_c": "c.4781G>C",
"hgvs_p": "p.Arg1594Pro",
"transcript": "XM_005268218.4",
"protein_id": "XP_005268275.1",
"transcript_support_level": null,
"aa_start": 1594,
"aa_end": null,
"aa_length": 1684,
"cds_start": 4781,
"cds_end": null,
"cds_length": 5055,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_005268218.4"
},
{
"aa_ref": "R",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 22,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NRXN3",
"gene_hgnc_id": 8010,
"hgvs_c": "c.4778G>C",
"hgvs_p": "p.Arg1593Pro",
"transcript": "XM_006720322.3",
"protein_id": "XP_006720385.1",
"transcript_support_level": null,
"aa_start": 1593,
"aa_end": null,
"aa_length": 1683,
"cds_start": 4778,
"cds_end": null,
"cds_length": 5052,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_006720322.3"
},
{
"aa_ref": "R",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 22,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NRXN3",
"gene_hgnc_id": 8010,
"hgvs_c": "c.4766G>C",
"hgvs_p": "p.Arg1589Pro",
"transcript": "XM_011537366.2",
"protein_id": "XP_011535668.1",
"transcript_support_level": null,
"aa_start": 1589,
"aa_end": null,
"aa_length": 1679,
"cds_start": 4766,
"cds_end": null,
"cds_length": 5040,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011537366.2"
},
{
"aa_ref": "R",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 22,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NRXN3",
"gene_hgnc_id": 8010,
"hgvs_c": "c.4757G>C",
"hgvs_p": "p.Arg1586Pro",
"transcript": "XM_047431939.1",
"protein_id": "XP_047287895.1",
"transcript_support_level": null,
"aa_start": 1586,
"aa_end": null,
"aa_length": 1676,
"cds_start": 4757,
"cds_end": null,
"cds_length": 5031,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047431939.1"
},
{
"aa_ref": "R",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NRXN3",
"gene_hgnc_id": 8010,
"hgvs_c": "c.4754G>C",
"hgvs_p": "p.Arg1585Pro",
"transcript": "XM_017021794.2",
"protein_id": "XP_016877283.1",
"transcript_support_level": null,
"aa_start": 1585,
"aa_end": null,
"aa_length": 1675,
"cds_start": 4754,
"cds_end": null,
"cds_length": 5028,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017021794.2"
},
{
"aa_ref": "R",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NRXN3",
"gene_hgnc_id": 8010,
"hgvs_c": "c.4745G>C",
"hgvs_p": "p.Arg1582Pro",
"transcript": "XM_047431940.1",
"protein_id": "XP_047287896.1",
"transcript_support_level": null,
"aa_start": 1582,
"aa_end": null,
"aa_length": 1672,
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}