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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: 10-72097363-C-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=10&pos=72097363&ref=C&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "10",
"pos": 72097363,
"ref": "C",
"alt": "A",
"effect": "missense_variant",
"transcript": "NM_001198798.2",
"consequences": [
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ASCC1",
"gene_hgnc_id": 24268,
"hgvs_c": "c.1045G>T",
"hgvs_p": "p.Ala349Ser",
"transcript": "NM_001198800.3",
"protein_id": "NP_001185729.1",
"transcript_support_level": null,
"aa_start": 349,
"aa_end": null,
"aa_length": 357,
"cds_start": 1045,
"cds_end": null,
"cds_length": 1074,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000672957.1",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001198800.3"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ASCC1",
"gene_hgnc_id": 24268,
"hgvs_c": "c.1045G>T",
"hgvs_p": "p.Ala349Ser",
"transcript": "ENST00000672957.1",
"protein_id": "ENSP00000500935.1",
"transcript_support_level": null,
"aa_start": 349,
"aa_end": null,
"aa_length": 357,
"cds_start": 1045,
"cds_end": null,
"cds_length": 1074,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_001198800.3",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000672957.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ASCC1",
"gene_hgnc_id": 24268,
"hgvs_c": "c.1129G>T",
"hgvs_p": "p.Ala377Ser",
"transcript": "ENST00000902262.1",
"protein_id": "ENSP00000572321.1",
"transcript_support_level": null,
"aa_start": 377,
"aa_end": null,
"aa_length": 385,
"cds_start": 1129,
"cds_end": null,
"cds_length": 1158,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000902262.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ASCC1",
"gene_hgnc_id": 24268,
"hgvs_c": "c.1105G>T",
"hgvs_p": "p.Ala369Ser",
"transcript": "ENST00000672774.1",
"protein_id": "ENSP00000500488.1",
"transcript_support_level": null,
"aa_start": 369,
"aa_end": null,
"aa_length": 377,
"cds_start": 1105,
"cds_end": null,
"cds_length": 1134,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000672774.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ASCC1",
"gene_hgnc_id": 24268,
"hgvs_c": "c.1105G>T",
"hgvs_p": "p.Ala369Ser",
"transcript": "ENST00000957305.1",
"protein_id": "ENSP00000627364.1",
"transcript_support_level": null,
"aa_start": 369,
"aa_end": null,
"aa_length": 377,
"cds_start": 1105,
"cds_end": null,
"cds_length": 1134,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000957305.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ASCC1",
"gene_hgnc_id": 24268,
"hgvs_c": "c.1045G>T",
"hgvs_p": "p.Ala349Ser",
"transcript": "NM_001198798.2",
"protein_id": "NP_001185727.1",
"transcript_support_level": null,
"aa_start": 349,
"aa_end": null,
"aa_length": 357,
"cds_start": 1045,
"cds_end": null,
"cds_length": 1074,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001198798.2"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ASCC1",
"gene_hgnc_id": 24268,
"hgvs_c": "c.1045G>T",
"hgvs_p": "p.Ala349Ser",
"transcript": "NM_001369093.1",
"protein_id": "NP_001356022.1",
"transcript_support_level": null,
"aa_start": 349,
"aa_end": null,
"aa_length": 357,
"cds_start": 1045,
"cds_end": null,
"cds_length": 1074,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001369093.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ASCC1",
"gene_hgnc_id": 24268,
"hgvs_c": "c.1045G>T",
"hgvs_p": "p.Ala349Ser",
"transcript": "NM_001369094.1",
"protein_id": "NP_001356023.1",
"transcript_support_level": null,
"aa_start": 349,
"aa_end": null,
"aa_length": 357,
"cds_start": 1045,
"cds_end": null,
"cds_length": 1074,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001369094.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ASCC1",
"gene_hgnc_id": 24268,
"hgvs_c": "c.1045G>T",
"hgvs_p": "p.Ala349Ser",
"transcript": "NM_001369095.1",
"protein_id": "NP_001356024.1",
"transcript_support_level": null,
"aa_start": 349,
"aa_end": null,
"aa_length": 357,
"cds_start": 1045,
"cds_end": null,
"cds_length": 1074,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001369095.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ASCC1",
"gene_hgnc_id": 24268,
"hgvs_c": "c.1045G>T",
"hgvs_p": "p.Ala349Ser",
"transcript": "ENST00000317126.8",
"protein_id": "ENSP00000320461.4",
"transcript_support_level": 2,
"aa_start": 349,
"aa_end": null,
"aa_length": 357,
"cds_start": 1045,
"cds_end": null,
"cds_length": 1074,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000317126.8"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ASCC1",
"gene_hgnc_id": 24268,
"hgvs_c": "c.1045G>T",
"hgvs_p": "p.Ala349Ser",
"transcript": "ENST00000902261.1",
"protein_id": "ENSP00000572320.1",
"transcript_support_level": null,
"aa_start": 349,
"aa_end": null,
"aa_length": 357,
"cds_start": 1045,
"cds_end": null,
"cds_length": 1074,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000902261.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ASCC1",
"gene_hgnc_id": 24268,
"hgvs_c": "c.1045G>T",
"hgvs_p": "p.Ala349Ser",
"transcript": "ENST00000902263.1",
"protein_id": "ENSP00000572322.1",
"transcript_support_level": null,
"aa_start": 349,
"aa_end": null,
"aa_length": 357,
"cds_start": 1045,
"cds_end": null,
"cds_length": 1074,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000902263.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ASCC1",
"gene_hgnc_id": 24268,
"hgvs_c": "c.1045G>T",
"hgvs_p": "p.Ala349Ser",
"transcript": "ENST00000902264.1",
"protein_id": "ENSP00000572323.1",
"transcript_support_level": null,
"aa_start": 349,
"aa_end": null,
"aa_length": 357,
"cds_start": 1045,
"cds_end": null,
"cds_length": 1074,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000902264.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ASCC1",
"gene_hgnc_id": 24268,
"hgvs_c": "c.1045G>T",
"hgvs_p": "p.Ala349Ser",
"transcript": "ENST00000911756.1",
"protein_id": "ENSP00000581815.1",
"transcript_support_level": null,
"aa_start": 349,
"aa_end": null,
"aa_length": 357,
"cds_start": 1045,
"cds_end": null,
"cds_length": 1074,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000911756.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ASCC1",
"gene_hgnc_id": 24268,
"hgvs_c": "c.1045G>T",
"hgvs_p": "p.Ala349Ser",
"transcript": "ENST00000957304.1",
"protein_id": "ENSP00000627363.1",
"transcript_support_level": null,
"aa_start": 349,
"aa_end": null,
"aa_length": 357,
"cds_start": 1045,
"cds_end": null,
"cds_length": 1074,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000957304.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ASCC1",
"gene_hgnc_id": 24268,
"hgvs_c": "c.991G>T",
"hgvs_p": "p.Ala331Ser",
"transcript": "NM_001369099.1",
"protein_id": "NP_001356028.1",
"transcript_support_level": null,
"aa_start": 331,
"aa_end": null,
"aa_length": 339,
"cds_start": 991,
"cds_end": null,
"cds_length": 1020,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001369099.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ASCC1",
"gene_hgnc_id": 24268,
"hgvs_c": "c.928G>T",
"hgvs_p": "p.Ala310Ser",
"transcript": "NM_001369105.1",
"protein_id": "NP_001356034.1",
"transcript_support_level": null,
"aa_start": 310,
"aa_end": null,
"aa_length": 318,
"cds_start": 928,
"cds_end": null,
"cds_length": 957,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001369105.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ASCC1",
"gene_hgnc_id": 24268,
"hgvs_c": "c.928G>T",
"hgvs_p": "p.Ala310Ser",
"transcript": "NM_001369106.1",
"protein_id": "NP_001356035.1",
"transcript_support_level": null,
"aa_start": 310,
"aa_end": null,
"aa_length": 318,
"cds_start": 928,
"cds_end": null,
"cds_length": 957,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001369106.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ASCC1",
"gene_hgnc_id": 24268,
"hgvs_c": "c.928G>T",
"hgvs_p": "p.Ala310Ser",
"transcript": "NM_001369107.1",
"protein_id": "NP_001356036.1",
"transcript_support_level": null,
"aa_start": 310,
"aa_end": null,
"aa_length": 318,
"cds_start": 928,
"cds_end": null,
"cds_length": 957,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001369107.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ASCC1",
"gene_hgnc_id": 24268,
"hgvs_c": "c.925G>T",
"hgvs_p": "p.Ala309Ser",
"transcript": "NM_001369108.1",
"protein_id": "NP_001356037.1",
"transcript_support_level": null,
"aa_start": 309,
"aa_end": null,
"aa_length": 317,
"cds_start": 925,
"cds_end": null,
"cds_length": 954,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001369108.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ASCC1",
"gene_hgnc_id": 24268,
"hgvs_c": "c.925G>T",
"hgvs_p": "p.Ala309Ser",
"transcript": "NM_001369109.1",
"protein_id": "NP_001356038.1",
"transcript_support_level": null,
"aa_start": 309,
"aa_end": null,
"aa_length": 317,
"cds_start": 925,
"cds_end": null,
"cds_length": 954,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001369109.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ASCC1",
"gene_hgnc_id": 24268,
"hgvs_c": "c.925G>T",
"hgvs_p": "p.Ala309Ser",
"transcript": "ENST00000672940.1",
"protein_id": "ENSP00000500074.1",
"transcript_support_level": null,
"aa_start": 309,
"aa_end": null,
"aa_length": 317,
"cds_start": 925,
"cds_end": null,
"cds_length": 954,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000672940.1"
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}
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}