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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: 3-185675413-T-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=3&pos=185675413&ref=T&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "3",
"pos": 185675413,
"ref": "T",
"alt": "C",
"effect": "missense_variant",
"transcript": "NM_001291869.3",
"consequences": [
{
"aa_ref": "I",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IGF2BP2",
"gene_hgnc_id": 28867,
"hgvs_c": "c.954A>G",
"hgvs_p": "p.Ile318Met",
"transcript": "NM_006548.6",
"protein_id": "NP_006539.3",
"transcript_support_level": null,
"aa_start": 318,
"aa_end": null,
"aa_length": 599,
"cds_start": 954,
"cds_end": null,
"cds_length": 1800,
"cdna_start": 1036,
"cdna_end": null,
"cdna_length": 4283,
"mane_select": "ENST00000382199.7",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_006548.6"
},
{
"aa_ref": "I",
"aa_alt": "M",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IGF2BP2",
"gene_hgnc_id": 28867,
"hgvs_c": "c.954A>G",
"hgvs_p": "p.Ile318Met",
"transcript": "ENST00000382199.7",
"protein_id": "ENSP00000371634.3",
"transcript_support_level": 1,
"aa_start": 318,
"aa_end": null,
"aa_length": 599,
"cds_start": 954,
"cds_end": null,
"cds_length": 1800,
"cdna_start": 1036,
"cdna_end": null,
"cdna_length": 4283,
"mane_select": "NM_006548.6",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000382199.7"
},
{
"aa_ref": "I",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IGF2BP2",
"gene_hgnc_id": 28867,
"hgvs_c": "c.954A>G",
"hgvs_p": "p.Ile318Met",
"transcript": "ENST00000346192.7",
"protein_id": "ENSP00000320204.5",
"transcript_support_level": 1,
"aa_start": 318,
"aa_end": null,
"aa_length": 556,
"cds_start": 954,
"cds_end": null,
"cds_length": 1671,
"cdna_start": 1018,
"cdna_end": null,
"cdna_length": 3291,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000346192.7"
},
{
"aa_ref": "I",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IGF2BP2",
"gene_hgnc_id": 28867,
"hgvs_c": "c.765A>G",
"hgvs_p": "p.Ile255Met",
"transcript": "ENST00000421047.3",
"protein_id": "ENSP00000413787.3",
"transcript_support_level": 1,
"aa_start": 255,
"aa_end": null,
"aa_length": 536,
"cds_start": 765,
"cds_end": null,
"cds_length": 1611,
"cdna_start": 835,
"cdna_end": null,
"cdna_length": 1711,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000421047.3"
},
{
"aa_ref": "I",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IGF2BP2",
"gene_hgnc_id": 28867,
"hgvs_c": "c.1143A>G",
"hgvs_p": "p.Ile381Met",
"transcript": "ENST00000881591.1",
"protein_id": "ENSP00000551650.1",
"transcript_support_level": null,
"aa_start": 381,
"aa_end": null,
"aa_length": 662,
"cds_start": 1143,
"cds_end": null,
"cds_length": 1989,
"cdna_start": 1244,
"cdna_end": null,
"cdna_length": 3211,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000881591.1"
},
{
"aa_ref": "I",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IGF2BP2",
"gene_hgnc_id": 28867,
"hgvs_c": "c.972A>G",
"hgvs_p": "p.Ile324Met",
"transcript": "NM_001291869.3",
"protein_id": "NP_001278798.1",
"transcript_support_level": null,
"aa_start": 324,
"aa_end": null,
"aa_length": 605,
"cds_start": 972,
"cds_end": null,
"cds_length": 1818,
"cdna_start": 1054,
"cdna_end": null,
"cdna_length": 4301,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001291869.3"
},
{
"aa_ref": "I",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IGF2BP2",
"gene_hgnc_id": 28867,
"hgvs_c": "c.972A>G",
"hgvs_p": "p.Ile324Met",
"transcript": "ENST00000457616.6",
"protein_id": "ENSP00000410242.2",
"transcript_support_level": 5,
"aa_start": 324,
"aa_end": null,
"aa_length": 605,
"cds_start": 972,
"cds_end": null,
"cds_length": 1818,
"cdna_start": 1024,
"cdna_end": null,
"cdna_length": 3426,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000457616.6"
},
{
"aa_ref": "I",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IGF2BP2",
"gene_hgnc_id": 28867,
"hgvs_c": "c.951A>G",
"hgvs_p": "p.Ile317Met",
"transcript": "ENST00000921331.1",
"protein_id": "ENSP00000591390.1",
"transcript_support_level": null,
"aa_start": 317,
"aa_end": null,
"aa_length": 598,
"cds_start": 951,
"cds_end": null,
"cds_length": 1797,
"cdna_start": 1030,
"cdna_end": null,
"cdna_length": 3667,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000921331.1"
},
{
"aa_ref": "I",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IGF2BP2",
"gene_hgnc_id": 28867,
"hgvs_c": "c.954A>G",
"hgvs_p": "p.Ile318Met",
"transcript": "ENST00000921330.1",
"protein_id": "ENSP00000591389.1",
"transcript_support_level": null,
"aa_start": 318,
"aa_end": null,
"aa_length": 587,
"cds_start": 954,
"cds_end": null,
"cds_length": 1764,
"cdna_start": 1035,
"cdna_end": null,
"cdna_length": 3637,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000921330.1"
},
{
"aa_ref": "I",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IGF2BP2",
"gene_hgnc_id": 28867,
"hgvs_c": "c.954A>G",
"hgvs_p": "p.Ile318Met",
"transcript": "ENST00000921333.1",
"protein_id": "ENSP00000591392.1",
"transcript_support_level": null,
"aa_start": 318,
"aa_end": null,
"aa_length": 576,
"cds_start": 954,
"cds_end": null,
"cds_length": 1731,
"cdna_start": 1032,
"cdna_end": null,
"cdna_length": 3597,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000921333.1"
},
{
"aa_ref": "I",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IGF2BP2",
"gene_hgnc_id": 28867,
"hgvs_c": "c.954A>G",
"hgvs_p": "p.Ile318Met",
"transcript": "ENST00000881590.1",
"protein_id": "ENSP00000551649.1",
"transcript_support_level": null,
"aa_start": 318,
"aa_end": null,
"aa_length": 574,
"cds_start": 954,
"cds_end": null,
"cds_length": 1725,
"cdna_start": 1001,
"cdna_end": null,
"cdna_length": 3328,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000881590.1"
},
{
"aa_ref": "I",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IGF2BP2",
"gene_hgnc_id": 28867,
"hgvs_c": "c.972A>G",
"hgvs_p": "p.Ile324Met",
"transcript": "ENST00000881588.1",
"protein_id": "ENSP00000551647.1",
"transcript_support_level": null,
"aa_start": 324,
"aa_end": null,
"aa_length": 562,
"cds_start": 972,
"cds_end": null,
"cds_length": 1689,
"cdna_start": 1035,
"cdna_end": null,
"cdna_length": 3308,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000881588.1"
},
{
"aa_ref": "I",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IGF2BP2",
"gene_hgnc_id": 28867,
"hgvs_c": "c.954A>G",
"hgvs_p": "p.Ile318Met",
"transcript": "NM_001007225.3",
"protein_id": "NP_001007226.1",
"transcript_support_level": null,
"aa_start": 318,
"aa_end": null,
"aa_length": 556,
"cds_start": 954,
"cds_end": null,
"cds_length": 1671,
"cdna_start": 1036,
"cdna_end": null,
"cdna_length": 4154,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001007225.3"
},
{
"aa_ref": "I",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IGF2BP2",
"gene_hgnc_id": 28867,
"hgvs_c": "c.951A>G",
"hgvs_p": "p.Ile317Met",
"transcript": "ENST00000881589.1",
"protein_id": "ENSP00000551648.1",
"transcript_support_level": null,
"aa_start": 317,
"aa_end": null,
"aa_length": 555,
"cds_start": 951,
"cds_end": null,
"cds_length": 1668,
"cdna_start": 1005,
"cdna_end": null,
"cdna_length": 3278,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000881589.1"
},
{
"aa_ref": "I",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IGF2BP2",
"gene_hgnc_id": 28867,
"hgvs_c": "c.954A>G",
"hgvs_p": "p.Ile318Met",
"transcript": "ENST00000921325.1",
"protein_id": "ENSP00000591384.1",
"transcript_support_level": null,
"aa_start": 318,
"aa_end": null,
"aa_length": 555,
"cds_start": 954,
"cds_end": null,
"cds_length": 1668,
"cdna_start": 1055,
"cdna_end": null,
"cdna_length": 3561,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000921325.1"
},
{
"aa_ref": "I",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IGF2BP2",
"gene_hgnc_id": 28867,
"hgvs_c": "c.948A>G",
"hgvs_p": "p.Ile316Met",
"transcript": "ENST00000955762.1",
"protein_id": "ENSP00000625821.1",
"transcript_support_level": null,
"aa_start": 316,
"aa_end": null,
"aa_length": 554,
"cds_start": 948,
"cds_end": null,
"cds_length": 1665,
"cdna_start": 1023,
"cdna_end": null,
"cdna_length": 3471,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000955762.1"
},
{
"aa_ref": "I",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IGF2BP2",
"gene_hgnc_id": 28867,
"hgvs_c": "c.789A>G",
"hgvs_p": "p.Ile263Met",
"transcript": "ENST00000921327.1",
"protein_id": "ENSP00000591386.1",
"transcript_support_level": null,
"aa_start": 263,
"aa_end": null,
"aa_length": 544,
"cds_start": 789,
"cds_end": null,
"cds_length": 1635,
"cdna_start": 876,
"cdna_end": null,
"cdna_length": 3512,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000921327.1"
},
{
"aa_ref": "I",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IGF2BP2",
"gene_hgnc_id": 28867,
"hgvs_c": "c.954A>G",
"hgvs_p": "p.Ile318Met",
"transcript": "ENST00000921335.1",
"protein_id": "ENSP00000591394.1",
"transcript_support_level": null,
"aa_start": 318,
"aa_end": null,
"aa_length": 544,
"cds_start": 954,
"cds_end": null,
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"cdna_start": 1013,
"cdna_end": null,
"cdna_length": 3485,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000921335.1"
},
{
"aa_ref": "I",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IGF2BP2",
"gene_hgnc_id": 28867,
"hgvs_c": "c.783A>G",
"hgvs_p": "p.Ile261Met",
"transcript": "NM_001291872.3",
"protein_id": "NP_001278801.1",
"transcript_support_level": null,
"aa_start": 261,
"aa_end": null,
"aa_length": 542,
"cds_start": 783,
"cds_end": null,
"cds_length": 1629,
"cdna_start": 864,
"cdna_end": null,
"cdna_length": 4111,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001291872.3"
},
{
"aa_ref": "I",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IGF2BP2",
"gene_hgnc_id": 28867,
"hgvs_c": "c.765A>G",
"hgvs_p": "p.Ile255Met",
"transcript": "NM_001291873.3",
"protein_id": "NP_001278802.1",
"transcript_support_level": null,
"aa_start": 255,
"aa_end": null,
"aa_length": 536,
"cds_start": 765,
"cds_end": null,
"cds_length": 1611,
"cdna_start": 846,
"cdna_end": null,
"cdna_length": 4093,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001291873.3"
},
{
"aa_ref": "I",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IGF2BP2",
"gene_hgnc_id": 28867,
"hgvs_c": "c.954A>G",
"hgvs_p": "p.Ile318Met",
"transcript": "ENST00000921326.1",
"protein_id": "ENSP00000591385.1",
"transcript_support_level": null,
"aa_start": 318,
"aa_end": null,
"aa_length": 512,
"cds_start": 954,
"cds_end": null,
"cds_length": 1539,
"cdna_start": 1046,
"cdna_end": null,
"cdna_length": 3423,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000921326.1"
},
{
"aa_ref": "I",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IGF2BP2",
"gene_hgnc_id": 28867,
"hgvs_c": "c.792A>G",
"hgvs_p": "p.Ile264Met",
"transcript": "ENST00000921337.1",
"protein_id": "ENSP00000591396.1",
"transcript_support_level": null,
"aa_start": 264,
"aa_end": null,
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"phenotype_combined": "not specified",
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}
],
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}