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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: 12-62535626-C-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=12&pos=62535626&ref=C&alt=G&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "12",
"pos": 62535626,
"ref": "C",
"alt": "G",
"effect": "missense_variant",
"transcript": "NM_015026.3",
"consequences": [
{
"aa_ref": "T",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 35,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MON2",
"gene_hgnc_id": 29177,
"hgvs_c": "c.1817C>G",
"hgvs_p": "p.Thr606Ser",
"transcript": "NM_015026.3",
"protein_id": "NP_055841.2",
"transcript_support_level": null,
"aa_start": 606,
"aa_end": null,
"aa_length": 1717,
"cds_start": 1817,
"cds_end": null,
"cds_length": 5154,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000393630.8",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_015026.3"
},
{
"aa_ref": "T",
"aa_alt": "S",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 35,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MON2",
"gene_hgnc_id": 29177,
"hgvs_c": "c.1817C>G",
"hgvs_p": "p.Thr606Ser",
"transcript": "ENST00000393630.8",
"protein_id": "ENSP00000377250.4",
"transcript_support_level": 1,
"aa_start": 606,
"aa_end": null,
"aa_length": 1717,
"cds_start": 1817,
"cds_end": null,
"cds_length": 5154,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_015026.3",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000393630.8"
},
{
"aa_ref": "T",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 34,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MON2",
"gene_hgnc_id": 29177,
"hgvs_c": "c.1817C>G",
"hgvs_p": "p.Thr606Ser",
"transcript": "ENST00000393629.6",
"protein_id": "ENSP00000377249.2",
"transcript_support_level": 1,
"aa_start": 606,
"aa_end": null,
"aa_length": 1711,
"cds_start": 1817,
"cds_end": null,
"cds_length": 5136,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000393629.6"
},
{
"aa_ref": "T",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 34,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MON2",
"gene_hgnc_id": 29177,
"hgvs_c": "c.1817C>G",
"hgvs_p": "p.Thr606Ser",
"transcript": "ENST00000552738.5",
"protein_id": "ENSP00000449215.1",
"transcript_support_level": 1,
"aa_start": 606,
"aa_end": null,
"aa_length": 1688,
"cds_start": 1817,
"cds_end": null,
"cds_length": 5067,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000552738.5"
},
{
"aa_ref": "T",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 36,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MON2",
"gene_hgnc_id": 29177,
"hgvs_c": "c.1817C>G",
"hgvs_p": "p.Thr606Ser",
"transcript": "ENST00000546600.5",
"protein_id": "ENSP00000447407.1",
"transcript_support_level": 1,
"aa_start": 606,
"aa_end": null,
"aa_length": 1675,
"cds_start": 1817,
"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": "ENST00000546600.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 36,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MON2",
"gene_hgnc_id": 29177,
"hgvs_c": "n.*1763C>G",
"hgvs_p": null,
"transcript": "ENST00000547095.5",
"protein_id": "ENSP00000446626.1",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000547095.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 36,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MON2",
"gene_hgnc_id": 29177,
"hgvs_c": "n.*1763C>G",
"hgvs_p": null,
"transcript": "ENST00000547095.5",
"protein_id": "ENSP00000446626.1",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000547095.5"
},
{
"aa_ref": "T",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 36,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MON2",
"gene_hgnc_id": 29177,
"hgvs_c": "c.1817C>G",
"hgvs_p": "p.Thr606Ser",
"transcript": "ENST00000641654.1",
"protein_id": "ENSP00000493462.1",
"transcript_support_level": null,
"aa_start": 606,
"aa_end": null,
"aa_length": 1718,
"cds_start": 1817,
"cds_end": null,
"cds_length": 5157,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000641654.1"
},
{
"aa_ref": "T",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 34,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MON2",
"gene_hgnc_id": 29177,
"hgvs_c": "c.1817C>G",
"hgvs_p": "p.Thr606Ser",
"transcript": "NM_001278470.2",
"protein_id": "NP_001265399.1",
"transcript_support_level": null,
"aa_start": 606,
"aa_end": null,
"aa_length": 1711,
"cds_start": 1817,
"cds_end": null,
"cds_length": 5136,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001278470.2"
},
{
"aa_ref": "T",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 35,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MON2",
"gene_hgnc_id": 29177,
"hgvs_c": "c.1817C>G",
"hgvs_p": "p.Thr606Ser",
"transcript": "ENST00000953602.1",
"protein_id": "ENSP00000623661.1",
"transcript_support_level": null,
"aa_start": 606,
"aa_end": null,
"aa_length": 1694,
"cds_start": 1817,
"cds_end": null,
"cds_length": 5085,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000953602.1"
},
{
"aa_ref": "T",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 34,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MON2",
"gene_hgnc_id": 29177,
"hgvs_c": "c.1817C>G",
"hgvs_p": "p.Thr606Ser",
"transcript": "NM_001278471.2",
"protein_id": "NP_001265400.1",
"transcript_support_level": null,
"aa_start": 606,
"aa_end": null,
"aa_length": 1688,
"cds_start": 1817,
"cds_end": null,
"cds_length": 5067,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001278471.2"
},
{
"aa_ref": "T",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 34,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MON2",
"gene_hgnc_id": 29177,
"hgvs_c": "c.1817C>G",
"hgvs_p": "p.Thr606Ser",
"transcript": "ENST00000953603.1",
"protein_id": "ENSP00000623662.1",
"transcript_support_level": null,
"aa_start": 606,
"aa_end": null,
"aa_length": 1683,
"cds_start": 1817,
"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": "ENST00000953603.1"
},
{
"aa_ref": "T",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 33,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MON2",
"gene_hgnc_id": 29177,
"hgvs_c": "c.1817C>G",
"hgvs_p": "p.Thr606Ser",
"transcript": "ENST00000854043.1",
"protein_id": "ENSP00000524102.1",
"transcript_support_level": null,
"aa_start": 606,
"aa_end": null,
"aa_length": 1677,
"cds_start": 1817,
"cds_end": null,
"cds_length": 5034,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000854043.1"
},
{
"aa_ref": "T",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 36,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MON2",
"gene_hgnc_id": 29177,
"hgvs_c": "c.1817C>G",
"hgvs_p": "p.Thr606Ser",
"transcript": "NM_001278469.3",
"protein_id": "NP_001265398.1",
"transcript_support_level": null,
"aa_start": 606,
"aa_end": null,
"aa_length": 1675,
"cds_start": 1817,
"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": "NM_001278469.3"
},
{
"aa_ref": "T",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 33,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MON2",
"gene_hgnc_id": 29177,
"hgvs_c": "c.1817C>G",
"hgvs_p": "p.Thr606Ser",
"transcript": "ENST00000914365.1",
"protein_id": "ENSP00000584424.1",
"transcript_support_level": null,
"aa_start": 606,
"aa_end": null,
"aa_length": 1668,
"cds_start": 1817,
"cds_end": null,
"cds_length": 5007,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000914365.1"
},
{
"aa_ref": "T",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 33,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MON2",
"gene_hgnc_id": 29177,
"hgvs_c": "c.1622C>G",
"hgvs_p": "p.Thr541Ser",
"transcript": "ENST00000854042.1",
"protein_id": "ENSP00000524101.1",
"transcript_support_level": null,
"aa_start": 541,
"aa_end": null,
"aa_length": 1646,
"cds_start": 1622,
"cds_end": null,
"cds_length": 4941,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000854042.1"
},
{
"aa_ref": "T",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 36,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MON2",
"gene_hgnc_id": 29177,
"hgvs_c": "c.1601C>G",
"hgvs_p": "p.Thr534Ser",
"transcript": "NM_001278472.2",
"protein_id": "NP_001265401.1",
"transcript_support_level": null,
"aa_start": 534,
"aa_end": null,
"aa_length": 1645,
"cds_start": 1601,
"cds_end": null,
"cds_length": 4938,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001278472.2"
},
{
"aa_ref": "T",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 33,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MON2",
"gene_hgnc_id": 29177,
"hgvs_c": "c.1817C>G",
"hgvs_p": "p.Thr606Ser",
"transcript": "ENST00000953601.1",
"protein_id": "ENSP00000623660.1",
"transcript_support_level": null,
"aa_start": 606,
"aa_end": null,
"aa_length": 1633,
"cds_start": 1817,
"cds_end": null,
"cds_length": 4902,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000953601.1"
},
{
"aa_ref": "T",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 32,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MON2",
"gene_hgnc_id": 29177,
"hgvs_c": "c.1817C>G",
"hgvs_p": "p.Thr606Ser",
"transcript": "ENST00000854041.1",
"protein_id": "ENSP00000524100.1",
"transcript_support_level": null,
"aa_start": 606,
"aa_end": null,
"aa_length": 1627,
"cds_start": 1817,
"cds_end": null,
"cds_length": 4884,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000854041.1"
},
{
"aa_ref": "T",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MON2",
"gene_hgnc_id": 29177,
"hgvs_c": "c.1817C>G",
"hgvs_p": "p.Thr606Ser",
"transcript": "ENST00000552115.5",
"protein_id": "ENSP00000446635.1",
"transcript_support_level": 5,
"aa_start": 606,
"aa_end": null,
"aa_length": 1072,
"cds_start": 1817,
"cds_end": null,
"cds_length": 3219,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000552115.5"
},
{
"aa_ref": "T",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 36,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MON2",
"gene_hgnc_id": 29177,
"hgvs_c": "c.1817C>G",
"hgvs_p": "p.Thr606Ser",
"transcript": "XM_017019041.2",
"protein_id": "XP_016874530.1",
"transcript_support_level": null,
"aa_start": 606,
"aa_end": null,
"aa_length": 1718,
"cds_start": 1817,
"cds_end": null,
"cds_length": 5157,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017019041.2"
},
{
"aa_ref": "T",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 35,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MON2",
"gene_hgnc_id": 29177,
"hgvs_c": "c.1817C>G",
"hgvs_p": "p.Thr606Ser",
"transcript": "XM_017019042.2",
"protein_id": "XP_016874531.1",
"transcript_support_level": null,
"aa_start": 606,
"aa_end": null,
"aa_length": 1712,
"cds_start": 1817,
"cds_end": null,
"cds_length": 5139,
"cdna_start": null,
"cdna_end": null,
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}