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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: 6-135200357-G-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=6&pos=135200357&ref=G&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "6",
"pos": 135200357,
"ref": "G",
"alt": "T",
"effect": "missense_variant",
"transcript": "NM_001130173.2",
"consequences": [
{
"aa_ref": "G",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYB",
"gene_hgnc_id": 7545,
"hgvs_c": "c.1892G>T",
"hgvs_p": "p.Gly631Val",
"transcript": "NM_001130173.2",
"protein_id": "NP_001123645.1",
"transcript_support_level": null,
"aa_start": 631,
"aa_end": null,
"aa_length": 761,
"cds_start": 1892,
"cds_end": null,
"cds_length": 2286,
"cdna_start": 2098,
"cdna_end": null,
"cdna_length": 3684,
"mane_select": "ENST00000341911.10",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001130173.2"
},
{
"aa_ref": "G",
"aa_alt": "V",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYB",
"gene_hgnc_id": 7545,
"hgvs_c": "c.1892G>T",
"hgvs_p": "p.Gly631Val",
"transcript": "ENST00000341911.10",
"protein_id": "ENSP00000339992.5",
"transcript_support_level": 1,
"aa_start": 631,
"aa_end": null,
"aa_length": 761,
"cds_start": 1892,
"cds_end": null,
"cds_length": 2286,
"cdna_start": 2098,
"cdna_end": null,
"cdna_length": 3684,
"mane_select": "NM_001130173.2",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000341911.10"
},
{
"aa_ref": "G",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYB",
"gene_hgnc_id": 7545,
"hgvs_c": "c.1883G>T",
"hgvs_p": "p.Gly628Val",
"transcript": "ENST00000528774.5",
"protein_id": "ENSP00000434723.1",
"transcript_support_level": 1,
"aa_start": 628,
"aa_end": null,
"aa_length": 758,
"cds_start": 1883,
"cds_end": null,
"cds_length": 2277,
"cdna_start": 1883,
"cdna_end": null,
"cdna_length": 2277,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000528774.5"
},
{
"aa_ref": "G",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYB",
"gene_hgnc_id": 7545,
"hgvs_c": "c.1844G>T",
"hgvs_p": "p.Gly615Val",
"transcript": "ENST00000534121.5",
"protein_id": "ENSP00000432851.1",
"transcript_support_level": 1,
"aa_start": 615,
"aa_end": null,
"aa_length": 745,
"cds_start": 1844,
"cds_end": null,
"cds_length": 2238,
"cdna_start": 1844,
"cdna_end": null,
"cdna_length": 2238,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000534121.5"
},
{
"aa_ref": "G",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYB",
"gene_hgnc_id": 7545,
"hgvs_c": "c.1529G>T",
"hgvs_p": "p.Gly510Val",
"transcript": "ENST00000367814.8",
"protein_id": "ENSP00000356788.4",
"transcript_support_level": 1,
"aa_start": 510,
"aa_end": null,
"aa_length": 640,
"cds_start": 1529,
"cds_end": null,
"cds_length": 1923,
"cdna_start": 1715,
"cdna_end": null,
"cdna_length": 3302,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000367814.8"
},
{
"aa_ref": "G",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYB",
"gene_hgnc_id": 7545,
"hgvs_c": "c.1520G>T",
"hgvs_p": "p.Gly507Val",
"transcript": "ENST00000442647.7",
"protein_id": "ENSP00000410825.2",
"transcript_support_level": 1,
"aa_start": 507,
"aa_end": null,
"aa_length": 637,
"cds_start": 1520,
"cds_end": null,
"cds_length": 1914,
"cdna_start": 1726,
"cdna_end": null,
"cdna_length": 3312,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000442647.7"
},
{
"aa_ref": "G",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYB",
"gene_hgnc_id": 7545,
"hgvs_c": "c.1424G>T",
"hgvs_p": "p.Gly475Val",
"transcript": "ENST00000533624.5",
"protein_id": "ENSP00000436605.1",
"transcript_support_level": 1,
"aa_start": 475,
"aa_end": null,
"aa_length": 605,
"cds_start": 1424,
"cds_end": null,
"cds_length": 1818,
"cdna_start": 1424,
"cdna_end": null,
"cdna_length": 1818,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000533624.5"
},
{
"aa_ref": "G",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYB",
"gene_hgnc_id": 7545,
"hgvs_c": "c.1529G>T",
"hgvs_p": "p.Gly510Val",
"transcript": "ENST00000534044.5",
"protein_id": "ENSP00000435055.1",
"transcript_support_level": 1,
"aa_start": 510,
"aa_end": null,
"aa_length": 603,
"cds_start": 1529,
"cds_end": null,
"cds_length": 1812,
"cdna_start": 1529,
"cdna_end": null,
"cdna_length": 1812,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000534044.5"
},
{
"aa_ref": "G",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYB",
"gene_hgnc_id": 7545,
"hgvs_c": "c.1274G>T",
"hgvs_p": "p.Gly425Val",
"transcript": "ENST00000525369.5",
"protein_id": "ENSP00000435938.1",
"transcript_support_level": 1,
"aa_start": 425,
"aa_end": null,
"aa_length": 555,
"cds_start": 1274,
"cds_end": null,
"cds_length": 1668,
"cdna_start": 1280,
"cdna_end": null,
"cdna_length": 2866,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000525369.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYB",
"gene_hgnc_id": 7545,
"hgvs_c": "n.*235G>T",
"hgvs_p": null,
"transcript": "ENST00000339290.9",
"protein_id": "ENSP00000341050.5",
"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": 3365,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000339290.9"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYB",
"gene_hgnc_id": 7545,
"hgvs_c": "n.1529G>T",
"hgvs_p": null,
"transcript": "ENST00000367812.6",
"protein_id": "ENSP00000356786.2",
"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": 3565,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000367812.6"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYB",
"gene_hgnc_id": 7545,
"hgvs_c": "n.*235G>T",
"hgvs_p": null,
"transcript": "ENST00000438901.6",
"protein_id": "ENSP00000413011.2",
"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": 3481,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000438901.6"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYB",
"gene_hgnc_id": 7545,
"hgvs_c": "n.*598G>T",
"hgvs_p": null,
"transcript": "ENST00000463282.6",
"protein_id": "ENSP00000436602.1",
"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": 3422,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000463282.6"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYB",
"gene_hgnc_id": 7545,
"hgvs_c": "n.*996G>T",
"hgvs_p": null,
"transcript": "ENST00000524588.5",
"protein_id": "ENSP00000434675.1",
"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": 1630,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000524588.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYB",
"gene_hgnc_id": 7545,
"hgvs_c": "n.1529G>T",
"hgvs_p": null,
"transcript": "ENST00000525002.5",
"protein_id": "ENSP00000433745.1",
"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": 2182,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000525002.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYB",
"gene_hgnc_id": 7545,
"hgvs_c": "n.*598G>T",
"hgvs_p": null,
"transcript": "ENST00000525477.5",
"protein_id": "ENSP00000437081.1",
"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": 3431,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000525477.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYB",
"gene_hgnc_id": 7545,
"hgvs_c": "n.*654G>T",
"hgvs_p": null,
"transcript": "ENST00000525514.5",
"protein_id": "ENSP00000435578.1",
"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": 3288,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000525514.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYB",
"gene_hgnc_id": 7545,
"hgvs_c": "n.*319G>T",
"hgvs_p": null,
"transcript": "ENST00000525940.5",
"protein_id": "ENSP00000432948.1",
"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": 1838,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000525940.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYB",
"gene_hgnc_id": 7545,
"hgvs_c": "n.*538G>T",
"hgvs_p": null,
"transcript": "ENST00000526187.5",
"protein_id": "ENSP00000434795.1",
"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": 2192,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000526187.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYB",
"gene_hgnc_id": 7545,
"hgvs_c": "n.*375G>T",
"hgvs_p": null,
"transcript": "ENST00000526320.5",
"protein_id": "ENSP00000434917.1",
"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": 3081,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000526320.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYB",
"gene_hgnc_id": 7545,
"hgvs_c": "n.*961G>T",
"hgvs_p": null,
"transcript": "ENST00000526565.5",
"protein_id": "ENSP00000436385.1",
"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": 2399,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000526565.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYB",
"gene_hgnc_id": 7545,
"hgvs_c": "n.*235G>T",
"hgvs_p": null,
"transcript": "ENST00000526889.5",
"protein_id": "ENSP00000433458.1",
"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": 3157,
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}
],
"message": null
}