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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: 1-161209915-C-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=1&pos=161209915&ref=C&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "1",
"pos": 161209915,
"ref": "C",
"alt": "A",
"effect": "missense_variant",
"transcript": "ENST00000676972.1",
"consequences": [
{
"aa_ref": "P",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDUFS2",
"gene_hgnc_id": 7708,
"hgvs_c": "c.686C>A",
"hgvs_p": "p.Pro229Gln",
"transcript": "NM_001377299.1",
"protein_id": "NP_001364228.1",
"transcript_support_level": null,
"aa_start": 229,
"aa_end": null,
"aa_length": 463,
"cds_start": 686,
"cds_end": null,
"cds_length": 1392,
"cdna_start": 705,
"cdna_end": null,
"cdna_length": 1613,
"mane_select": "ENST00000676972.1",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "Q",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDUFS2",
"gene_hgnc_id": 7708,
"hgvs_c": "c.686C>A",
"hgvs_p": "p.Pro229Gln",
"transcript": "ENST00000676972.1",
"protein_id": "ENSP00000503117.1",
"transcript_support_level": null,
"aa_start": 229,
"aa_end": null,
"aa_length": 463,
"cds_start": 686,
"cds_end": null,
"cds_length": 1392,
"cdna_start": 705,
"cdna_end": null,
"cdna_length": 1613,
"mane_select": "NM_001377299.1",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDUFS2",
"gene_hgnc_id": 7708,
"hgvs_c": "c.686C>A",
"hgvs_p": "p.Pro229Gln",
"transcript": "ENST00000367993.7",
"protein_id": "ENSP00000356972.3",
"transcript_support_level": 1,
"aa_start": 229,
"aa_end": null,
"aa_length": 463,
"cds_start": 686,
"cds_end": null,
"cds_length": 1392,
"cdna_start": 1134,
"cdna_end": null,
"cdna_length": 2042,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDUFS2",
"gene_hgnc_id": 7708,
"hgvs_c": "c.686C>A",
"hgvs_p": "p.Pro229Gln",
"transcript": "ENST00000392179.5",
"protein_id": "ENSP00000376018.4",
"transcript_support_level": 1,
"aa_start": 229,
"aa_end": null,
"aa_length": 457,
"cds_start": 686,
"cds_end": null,
"cds_length": 1374,
"cdna_start": 925,
"cdna_end": null,
"cdna_length": 2067,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDUFS2",
"gene_hgnc_id": 7708,
"hgvs_c": "c.686C>A",
"hgvs_p": "p.Pro229Gln",
"transcript": "ENST00000677453.1",
"protein_id": "ENSP00000503604.1",
"transcript_support_level": null,
"aa_start": 229,
"aa_end": null,
"aa_length": 484,
"cds_start": 686,
"cds_end": null,
"cds_length": 1455,
"cdna_start": 802,
"cdna_end": null,
"cdna_length": 1889,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDUFS2",
"gene_hgnc_id": 7708,
"hgvs_c": "c.686C>A",
"hgvs_p": "p.Pro229Gln",
"transcript": "ENST00000677846.1",
"protein_id": "ENSP00000504065.1",
"transcript_support_level": null,
"aa_start": 229,
"aa_end": null,
"aa_length": 484,
"cds_start": 686,
"cds_end": null,
"cds_length": 1455,
"cdna_start": 989,
"cdna_end": null,
"cdna_length": 1939,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDUFS2",
"gene_hgnc_id": 7708,
"hgvs_c": "c.686C>A",
"hgvs_p": "p.Pro229Gln",
"transcript": "ENST00000677579.1",
"protein_id": "ENSP00000504162.1",
"transcript_support_level": null,
"aa_start": 229,
"aa_end": null,
"aa_length": 478,
"cds_start": 686,
"cds_end": null,
"cds_length": 1437,
"cdna_start": 989,
"cdna_end": null,
"cdna_length": 2092,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDUFS2",
"gene_hgnc_id": 7708,
"hgvs_c": "c.686C>A",
"hgvs_p": "p.Pro229Gln",
"transcript": "NM_001377298.1",
"protein_id": "NP_001364227.1",
"transcript_support_level": null,
"aa_start": 229,
"aa_end": null,
"aa_length": 463,
"cds_start": 686,
"cds_end": null,
"cds_length": 1392,
"cdna_start": 996,
"cdna_end": null,
"cdna_length": 1904,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDUFS2",
"gene_hgnc_id": 7708,
"hgvs_c": "c.686C>A",
"hgvs_p": "p.Pro229Gln",
"transcript": "NM_004550.5",
"protein_id": "NP_004541.1",
"transcript_support_level": null,
"aa_start": 229,
"aa_end": null,
"aa_length": 463,
"cds_start": 686,
"cds_end": null,
"cds_length": 1392,
"cdna_start": 1134,
"cdna_end": null,
"cdna_length": 2042,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDUFS2",
"gene_hgnc_id": 7708,
"hgvs_c": "c.686C>A",
"hgvs_p": "p.Pro229Gln",
"transcript": "ENST00000676600.1",
"protein_id": "ENSP00000503989.1",
"transcript_support_level": null,
"aa_start": 229,
"aa_end": null,
"aa_length": 463,
"cds_start": 686,
"cds_end": null,
"cds_length": 1392,
"cdna_start": 852,
"cdna_end": null,
"cdna_length": 1746,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDUFS2",
"gene_hgnc_id": 7708,
"hgvs_c": "c.686C>A",
"hgvs_p": "p.Pro229Gln",
"transcript": "ENST00000678507.1",
"protein_id": "ENSP00000504199.1",
"transcript_support_level": null,
"aa_start": 229,
"aa_end": null,
"aa_length": 463,
"cds_start": 686,
"cds_end": null,
"cds_length": 1392,
"cdna_start": 997,
"cdna_end": null,
"cdna_length": 1891,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDUFS2",
"gene_hgnc_id": 7708,
"hgvs_c": "c.686C>A",
"hgvs_p": "p.Pro229Gln",
"transcript": "ENST00000678511.1",
"protein_id": "ENSP00000504846.1",
"transcript_support_level": null,
"aa_start": 229,
"aa_end": null,
"aa_length": 463,
"cds_start": 686,
"cds_end": null,
"cds_length": 1392,
"cdna_start": 772,
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"cdna_length": 1666,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDUFS2",
"gene_hgnc_id": 7708,
"hgvs_c": "c.686C>A",
"hgvs_p": "p.Pro229Gln",
"transcript": "NM_001166159.2",
"protein_id": "NP_001159631.1",
"transcript_support_level": null,
"aa_start": 229,
"aa_end": null,
"aa_length": 457,
"cds_start": 686,
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"cds_length": 1374,
"cdna_start": 705,
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"cdna_length": 1847,
"mane_select": null,
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"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
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],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
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"gene_symbol": "NDUFS2",
"gene_hgnc_id": 7708,
"hgvs_c": "c.686C>A",
"hgvs_p": "p.Pro229Gln",
"transcript": "NM_001377300.1",
"protein_id": "NP_001364229.1",
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"mane_select": null,
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"feature": null
},
{
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"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDUFS2",
"gene_hgnc_id": 7708,
"hgvs_c": "c.686C>A",
"hgvs_p": "p.Pro229Gln",
"transcript": "NM_001377301.1",
"protein_id": "NP_001364230.1",
"transcript_support_level": null,
"aa_start": 229,
"aa_end": null,
"aa_length": 457,
"cds_start": 686,
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"cds_length": 1374,
"cdna_start": 1144,
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"cdna_length": 2286,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDUFS2",
"gene_hgnc_id": 7708,
"hgvs_c": "c.686C>A",
"hgvs_p": "p.Pro229Gln",
"transcript": "NM_001377302.1",
"protein_id": "NP_001364231.1",
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"mane_select": null,
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"biotype": null,
"feature": null
},
{
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"aa_alt": "Q",
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"protein_coding": true,
"strand": true,
"consequences": [
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],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDUFS2",
"gene_hgnc_id": 7708,
"hgvs_c": "c.686C>A",
"hgvs_p": "p.Pro229Gln",
"transcript": "ENST00000677550.1",
"protein_id": "ENSP00000503353.1",
"transcript_support_level": null,
"aa_start": 229,
"aa_end": null,
"aa_length": 457,
"cds_start": 686,
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"cdna_start": 1041,
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"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
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"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDUFS2",
"gene_hgnc_id": 7708,
"hgvs_c": "c.686C>A",
"hgvs_p": "p.Pro229Gln",
"transcript": "ENST00000679176.1",
"protein_id": "ENSP00000504170.1",
"transcript_support_level": null,
"aa_start": 229,
"aa_end": null,
"aa_length": 457,
"cds_start": 686,
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"cdna_start": 1137,
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"mane_select": null,
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},
{
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"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
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"gene_symbol": "NDUFS2",
"gene_hgnc_id": 7708,
"hgvs_c": "c.686C>A",
"hgvs_p": "p.Pro229Gln",
"transcript": "NM_001410889.1",
"protein_id": "NP_001397818.1",
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},
{
"aa_ref": "P",
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"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
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"gene_symbol": "NDUFS2",
"gene_hgnc_id": 7708,
"hgvs_c": "c.686C>A",
"hgvs_p": "p.Pro229Gln",
"transcript": "ENST00000678911.1",
"protein_id": "ENSP00000503946.1",
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"biotype": null,
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},
{
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"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
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"exon_count": 13,
"intron_rank": null,
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"gene_symbol": "NDUFS2",
"gene_hgnc_id": 7708,
"hgvs_c": "c.686C>A",
"hgvs_p": "p.Pro229Gln",
"transcript": "ENST00000677231.1",
"protein_id": "ENSP00000503378.1",
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"cds_start": 686,
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"cdna_start": 989,
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"mane_select": null,
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"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDUFS2",
"gene_hgnc_id": 7708,
"hgvs_c": "c.737C>A",
"hgvs_p": "p.Pro246Gln",
"transcript": "ENST00000679218.1",
"protein_id": "ENSP00000504577.1",
"transcript_support_level": null,
"aa_start": 246,
"aa_end": null,
"aa_length": 340,
"cds_start": 737,
"cds_end": null,
"cds_length": 1023,
"cdna_start": 774,
"cdna_end": null,
"cdna_length": 1060,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDUFS2",
"gene_hgnc_id": 7708,
"hgvs_c": "c.392C>A",
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}