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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: 2-240481047-C-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=240481047&ref=C&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "2",
"pos": 240481047,
"ref": "C",
"alt": "A",
"effect": "missense_variant",
"transcript": "NM_001282771.3",
"consequences": [
{
"aa_ref": "R",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ANKMY1",
"gene_hgnc_id": 20987,
"hgvs_c": "c.2936G>T",
"hgvs_p": "p.Arg979Leu",
"transcript": "NM_001282771.3",
"protein_id": "NP_001269700.1",
"transcript_support_level": null,
"aa_start": 979,
"aa_end": null,
"aa_length": 1030,
"cds_start": 2936,
"cds_end": null,
"cds_length": 3093,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000401804.6",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001282771.3"
},
{
"aa_ref": "R",
"aa_alt": "L",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ANKMY1",
"gene_hgnc_id": 20987,
"hgvs_c": "c.2936G>T",
"hgvs_p": "p.Arg979Leu",
"transcript": "ENST00000401804.6",
"protein_id": "ENSP00000385887.1",
"transcript_support_level": 1,
"aa_start": 979,
"aa_end": null,
"aa_length": 1030,
"cds_start": 2936,
"cds_end": null,
"cds_length": 3093,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_001282771.3",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000401804.6"
},
{
"aa_ref": "R",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ANKMY1",
"gene_hgnc_id": 20987,
"hgvs_c": "c.2669G>T",
"hgvs_p": "p.Arg890Leu",
"transcript": "ENST00000272972.7",
"protein_id": "ENSP00000272972.3",
"transcript_support_level": 1,
"aa_start": 890,
"aa_end": null,
"aa_length": 941,
"cds_start": 2669,
"cds_end": null,
"cds_length": 2826,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000272972.7"
},
{
"aa_ref": "R",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ANKMY1",
"gene_hgnc_id": 20987,
"hgvs_c": "c.2375G>T",
"hgvs_p": "p.Arg792Leu",
"transcript": "ENST00000403283.6",
"protein_id": "ENSP00000383968.1",
"transcript_support_level": 1,
"aa_start": 792,
"aa_end": null,
"aa_length": 843,
"cds_start": 2375,
"cds_end": null,
"cds_length": 2532,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000403283.6"
},
{
"aa_ref": "R",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ANKMY1",
"gene_hgnc_id": 20987,
"hgvs_c": "c.2006G>T",
"hgvs_p": "p.Arg669Leu",
"transcript": "ENST00000373318.6",
"protein_id": "ENSP00000362415.2",
"transcript_support_level": 1,
"aa_start": 669,
"aa_end": null,
"aa_length": 720,
"cds_start": 2006,
"cds_end": null,
"cds_length": 2163,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000373318.6"
},
{
"aa_ref": "R",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ANKMY1",
"gene_hgnc_id": 20987,
"hgvs_c": "c.1997G>T",
"hgvs_p": "p.Arg666Leu",
"transcript": "ENST00000361678.8",
"protein_id": "ENSP00000355097.4",
"transcript_support_level": 1,
"aa_start": 666,
"aa_end": null,
"aa_length": 717,
"cds_start": 1997,
"cds_end": null,
"cds_length": 2154,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000361678.8"
},
{
"aa_ref": "R",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ANKMY1",
"gene_hgnc_id": 20987,
"hgvs_c": "c.1952G>T",
"hgvs_p": "p.Arg651Leu",
"transcript": "ENST00000406958.5",
"protein_id": "ENSP00000384555.1",
"transcript_support_level": 1,
"aa_start": 651,
"aa_end": null,
"aa_length": 702,
"cds_start": 1952,
"cds_end": null,
"cds_length": 2109,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000406958.5"
},
{
"aa_ref": "R",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ANKMY1",
"gene_hgnc_id": 20987,
"hgvs_c": "c.2936G>T",
"hgvs_p": "p.Arg979Leu",
"transcript": "NM_001354023.3",
"protein_id": "NP_001340952.1",
"transcript_support_level": null,
"aa_start": 979,
"aa_end": null,
"aa_length": 1030,
"cds_start": 2936,
"cds_end": null,
"cds_length": 3093,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001354023.3"
},
{
"aa_ref": "R",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ANKMY1",
"gene_hgnc_id": 20987,
"hgvs_c": "c.2936G>T",
"hgvs_p": "p.Arg979Leu",
"transcript": "ENST00000959624.1",
"protein_id": "ENSP00000629683.1",
"transcript_support_level": null,
"aa_start": 979,
"aa_end": null,
"aa_length": 1030,
"cds_start": 2936,
"cds_end": null,
"cds_length": 3093,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000959624.1"
},
{
"aa_ref": "R",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ANKMY1",
"gene_hgnc_id": 20987,
"hgvs_c": "c.2852G>T",
"hgvs_p": "p.Arg951Leu",
"transcript": "NM_001393462.1",
"protein_id": "NP_001380391.1",
"transcript_support_level": null,
"aa_start": 951,
"aa_end": null,
"aa_length": 1002,
"cds_start": 2852,
"cds_end": null,
"cds_length": 3009,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001393462.1"
},
{
"aa_ref": "R",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ANKMY1",
"gene_hgnc_id": 20987,
"hgvs_c": "c.2687G>T",
"hgvs_p": "p.Arg896Leu",
"transcript": "ENST00000858022.1",
"protein_id": "ENSP00000528081.1",
"transcript_support_level": null,
"aa_start": 896,
"aa_end": null,
"aa_length": 947,
"cds_start": 2687,
"cds_end": null,
"cds_length": 2844,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000858022.1"
},
{
"aa_ref": "R",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ANKMY1",
"gene_hgnc_id": 20987,
"hgvs_c": "c.2669G>T",
"hgvs_p": "p.Arg890Leu",
"transcript": "NM_016552.5",
"protein_id": "NP_057636.2",
"transcript_support_level": null,
"aa_start": 890,
"aa_end": null,
"aa_length": 941,
"cds_start": 2669,
"cds_end": null,
"cds_length": 2826,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_016552.5"
},
{
"aa_ref": "R",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ANKMY1",
"gene_hgnc_id": 20987,
"hgvs_c": "c.2555G>T",
"hgvs_p": "p.Arg852Leu",
"transcript": "ENST00000858021.1",
"protein_id": "ENSP00000528080.1",
"transcript_support_level": null,
"aa_start": 852,
"aa_end": null,
"aa_length": 903,
"cds_start": 2555,
"cds_end": null,
"cds_length": 2712,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000858021.1"
},
{
"aa_ref": "R",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ANKMY1",
"gene_hgnc_id": 20987,
"hgvs_c": "c.2528G>T",
"hgvs_p": "p.Arg843Leu",
"transcript": "NM_001354024.3",
"protein_id": "NP_001340953.1",
"transcript_support_level": null,
"aa_start": 843,
"aa_end": null,
"aa_length": 894,
"cds_start": 2528,
"cds_end": null,
"cds_length": 2685,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001354024.3"
},
{
"aa_ref": "R",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ANKMY1",
"gene_hgnc_id": 20987,
"hgvs_c": "c.2375G>T",
"hgvs_p": "p.Arg792Leu",
"transcript": "NM_001308375.4",
"protein_id": "NP_001295304.3",
"transcript_support_level": null,
"aa_start": 792,
"aa_end": null,
"aa_length": 843,
"cds_start": 2375,
"cds_end": null,
"cds_length": 2532,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001308375.4"
},
{
"aa_ref": "R",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ANKMY1",
"gene_hgnc_id": 20987,
"hgvs_c": "c.2246G>T",
"hgvs_p": "p.Arg749Leu",
"transcript": "ENST00000858016.1",
"protein_id": "ENSP00000528075.1",
"transcript_support_level": null,
"aa_start": 749,
"aa_end": null,
"aa_length": 800,
"cds_start": 2246,
"cds_end": null,
"cds_length": 2403,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000858016.1"
},
{
"aa_ref": "R",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ANKMY1",
"gene_hgnc_id": 20987,
"hgvs_c": "c.2246G>T",
"hgvs_p": "p.Arg749Leu",
"transcript": "ENST00000858017.1",
"protein_id": "ENSP00000528076.1",
"transcript_support_level": null,
"aa_start": 749,
"aa_end": null,
"aa_length": 800,
"cds_start": 2246,
"cds_end": null,
"cds_length": 2403,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000858017.1"
},
{
"aa_ref": "R",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ANKMY1",
"gene_hgnc_id": 20987,
"hgvs_c": "c.2246G>T",
"hgvs_p": "p.Arg749Leu",
"transcript": "ENST00000858018.1",
"protein_id": "ENSP00000528077.1",
"transcript_support_level": null,
"aa_start": 749,
"aa_end": null,
"aa_length": 800,
"cds_start": 2246,
"cds_end": null,
"cds_length": 2403,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000858018.1"
},
{
"aa_ref": "R",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ANKMY1",
"gene_hgnc_id": 20987,
"hgvs_c": "c.1856G>T",
"hgvs_p": "p.Arg619Leu",
"transcript": "NM_001393464.1",
"protein_id": "NP_001380393.1",
"transcript_support_level": null,
"aa_start": 619,
"aa_end": null,
"aa_length": 771,
"cds_start": 1856,
"cds_end": null,
"cds_length": 2316,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001393464.1"
},
{
"aa_ref": "R",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ANKMY1",
"gene_hgnc_id": 20987,
"hgvs_c": "c.2138G>T",
"hgvs_p": "p.Arg713Leu",
"transcript": "ENST00000858019.1",
"protein_id": "ENSP00000528078.1",
"transcript_support_level": null,
"aa_start": 713,
"aa_end": null,
"aa_length": 764,
"cds_start": 2138,
"cds_end": null,
"cds_length": 2295,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000858019.1"
},
{
"aa_ref": "R",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ANKMY1",
"gene_hgnc_id": 20987,
"hgvs_c": "c.1730G>T",
"hgvs_p": "p.Arg577Leu",
"transcript": "NM_001393465.1",
"protein_id": "NP_001380394.1",
"transcript_support_level": null,
"aa_start": 577,
"aa_end": null,
"aa_length": 729,
"cds_start": 1730,
"cds_end": null,
"cds_length": 2190,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001393465.1"
},
{
"aa_ref": "R",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ANKMY1",
"gene_hgnc_id": 20987,
"hgvs_c": "c.2006G>T",
"hgvs_p": "p.Arg669Leu",
"transcript": "NM_001282780.2",
"protein_id": "NP_001269709.1",
"transcript_support_level": null,
"aa_start": 669,
"aa_end": null,
"aa_length": 720,
"cds_start": 2006,
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}