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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: 2-1943142-A-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=1943142&ref=A&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "2",
"pos": 1943142,
"ref": "A",
"alt": "T",
"effect": "missense_variant",
"transcript": "ENST00000647738.2",
"consequences": [
{
"aa_ref": "D",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYT1L",
"gene_hgnc_id": 7623,
"hgvs_c": "c.345T>A",
"hgvs_p": "p.Asp115Glu",
"transcript": "NM_001303052.2",
"protein_id": "NP_001289981.1",
"transcript_support_level": null,
"aa_start": 115,
"aa_end": null,
"aa_length": 1186,
"cds_start": 345,
"cds_end": null,
"cds_length": 3561,
"cdna_start": 1174,
"cdna_end": null,
"cdna_length": 7144,
"mane_select": "ENST00000647738.2",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "E",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYT1L",
"gene_hgnc_id": 7623,
"hgvs_c": "c.345T>A",
"hgvs_p": "p.Asp115Glu",
"transcript": "ENST00000647738.2",
"protein_id": "ENSP00000497479.2",
"transcript_support_level": null,
"aa_start": 115,
"aa_end": null,
"aa_length": 1186,
"cds_start": 345,
"cds_end": null,
"cds_length": 3561,
"cdna_start": 1174,
"cdna_end": null,
"cdna_length": 7144,
"mane_select": "NM_001303052.2",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYT1L",
"gene_hgnc_id": 7623,
"hgvs_c": "c.345T>A",
"hgvs_p": "p.Asp115Glu",
"transcript": "ENST00000428368.7",
"protein_id": "ENSP00000396103.3",
"transcript_support_level": 1,
"aa_start": 115,
"aa_end": null,
"aa_length": 1186,
"cds_start": 345,
"cds_end": null,
"cds_length": 3561,
"cdna_start": 1232,
"cdna_end": null,
"cdna_length": 6951,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYT1L",
"gene_hgnc_id": 7623,
"hgvs_c": "c.345T>A",
"hgvs_p": "p.Asp115Glu",
"transcript": "ENST00000399161.8",
"protein_id": "ENSP00000382114.3",
"transcript_support_level": 1,
"aa_start": 115,
"aa_end": null,
"aa_length": 1184,
"cds_start": 345,
"cds_end": null,
"cds_length": 3555,
"cdna_start": 1274,
"cdna_end": null,
"cdna_length": 7227,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYT1L",
"gene_hgnc_id": 7623,
"hgvs_c": "c.345T>A",
"hgvs_p": "p.Asp115Glu",
"transcript": "ENST00000644820.1",
"protein_id": "ENSP00000496210.1",
"transcript_support_level": null,
"aa_start": 115,
"aa_end": null,
"aa_length": 1207,
"cds_start": 345,
"cds_end": null,
"cds_length": 3624,
"cdna_start": 1247,
"cdna_end": null,
"cdna_length": 7269,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYT1L",
"gene_hgnc_id": 7623,
"hgvs_c": "c.345T>A",
"hgvs_p": "p.Asp115Glu",
"transcript": "NM_001329844.2",
"protein_id": "NP_001316773.1",
"transcript_support_level": null,
"aa_start": 115,
"aa_end": null,
"aa_length": 1186,
"cds_start": 345,
"cds_end": null,
"cds_length": 3561,
"cdna_start": 1250,
"cdna_end": null,
"cdna_length": 7220,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYT1L",
"gene_hgnc_id": 7623,
"hgvs_c": "c.345T>A",
"hgvs_p": "p.Asp115Glu",
"transcript": "NM_001329845.1",
"protein_id": "NP_001316774.1",
"transcript_support_level": null,
"aa_start": 115,
"aa_end": null,
"aa_length": 1186,
"cds_start": 345,
"cds_end": null,
"cds_length": 3561,
"cdna_start": 1040,
"cdna_end": null,
"cdna_length": 7010,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYT1L",
"gene_hgnc_id": 7623,
"hgvs_c": "c.345T>A",
"hgvs_p": "p.Asp115Glu",
"transcript": "ENST00000647694.1",
"protein_id": "ENSP00000497722.1",
"transcript_support_level": null,
"aa_start": 115,
"aa_end": null,
"aa_length": 1186,
"cds_start": 345,
"cds_end": null,
"cds_length": 3561,
"cdna_start": 1040,
"cdna_end": null,
"cdna_length": 6804,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYT1L",
"gene_hgnc_id": 7623,
"hgvs_c": "c.345T>A",
"hgvs_p": "p.Asp115Glu",
"transcript": "ENST00000650485.2",
"protein_id": "ENSP00000497068.1",
"transcript_support_level": null,
"aa_start": 115,
"aa_end": null,
"aa_length": 1186,
"cds_start": 345,
"cds_end": null,
"cds_length": 3561,
"cdna_start": 1246,
"cdna_end": null,
"cdna_length": 7178,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYT1L",
"gene_hgnc_id": 7623,
"hgvs_c": "c.345T>A",
"hgvs_p": "p.Asp115Glu",
"transcript": "ENST00000650560.1",
"protein_id": "ENSP00000497816.1",
"transcript_support_level": null,
"aa_start": 115,
"aa_end": null,
"aa_length": 1185,
"cds_start": 345,
"cds_end": null,
"cds_length": 3558,
"cdna_start": 1156,
"cdna_end": null,
"cdna_length": 7067,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYT1L",
"gene_hgnc_id": 7623,
"hgvs_c": "c.345T>A",
"hgvs_p": "p.Asp115Glu",
"transcript": "NM_001329847.2",
"protein_id": "NP_001316776.1",
"transcript_support_level": null,
"aa_start": 115,
"aa_end": null,
"aa_length": 1184,
"cds_start": 345,
"cds_end": null,
"cds_length": 3555,
"cdna_start": 1141,
"cdna_end": null,
"cdna_length": 7105,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYT1L",
"gene_hgnc_id": 7623,
"hgvs_c": "c.345T>A",
"hgvs_p": "p.Asp115Glu",
"transcript": "NM_001329848.1",
"protein_id": "NP_001316777.1",
"transcript_support_level": null,
"aa_start": 115,
"aa_end": null,
"aa_length": 1184,
"cds_start": 345,
"cds_end": null,
"cds_length": 3555,
"cdna_start": 1223,
"cdna_end": null,
"cdna_length": 7187,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYT1L",
"gene_hgnc_id": 7623,
"hgvs_c": "c.345T>A",
"hgvs_p": "p.Asp115Glu",
"transcript": "NM_015025.4",
"protein_id": "NP_055840.2",
"transcript_support_level": null,
"aa_start": 115,
"aa_end": null,
"aa_length": 1184,
"cds_start": 345,
"cds_end": null,
"cds_length": 3555,
"cdna_start": 1174,
"cdna_end": null,
"cdna_length": 7138,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYT1L",
"gene_hgnc_id": 7623,
"hgvs_c": "c.345T>A",
"hgvs_p": "p.Asp115Glu",
"transcript": "ENST00000648316.1",
"protein_id": "ENSP00000497870.1",
"transcript_support_level": null,
"aa_start": 115,
"aa_end": null,
"aa_length": 1184,
"cds_start": 345,
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"cdna_start": 1299,
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"mane_select": null,
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"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYT1L",
"gene_hgnc_id": 7623,
"hgvs_c": "c.345T>A",
"hgvs_p": "p.Asp115Glu",
"transcript": "ENST00000648928.1",
"protein_id": "ENSP00000497017.1",
"transcript_support_level": null,
"aa_start": 115,
"aa_end": null,
"aa_length": 1184,
"cds_start": 345,
"cds_end": null,
"cds_length": 3555,
"cdna_start": 1384,
"cdna_end": null,
"cdna_length": 7322,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYT1L",
"gene_hgnc_id": 7623,
"hgvs_c": "c.345T>A",
"hgvs_p": "p.Asp115Glu",
"transcript": "ENST00000649207.1",
"protein_id": "ENSP00000496986.1",
"transcript_support_level": null,
"aa_start": 115,
"aa_end": null,
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"cdna_start": 1246,
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"mane_select": null,
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"biotype": null,
"feature": null
},
{
"aa_ref": "D",
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"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYT1L",
"gene_hgnc_id": 7623,
"hgvs_c": "c.345T>A",
"hgvs_p": "p.Asp115Glu",
"transcript": "NM_001329849.3",
"protein_id": "NP_001316778.1",
"transcript_support_level": null,
"aa_start": 115,
"aa_end": null,
"aa_length": 1148,
"cds_start": 345,
"cds_end": null,
"cds_length": 3447,
"cdna_start": 1174,
"cdna_end": null,
"cdna_length": 6376,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYT1L",
"gene_hgnc_id": 7623,
"hgvs_c": "c.345T>A",
"hgvs_p": "p.Asp115Glu",
"transcript": "ENST00000648665.2",
"protein_id": "ENSP00000497115.1",
"transcript_support_level": null,
"aa_start": 115,
"aa_end": null,
"aa_length": 1148,
"cds_start": 345,
"cds_end": null,
"cds_length": 3447,
"cdna_start": 1156,
"cdna_end": null,
"cdna_length": 6155,
"mane_select": null,
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"biotype": null,
"feature": null
},
{
"aa_ref": "D",
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"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYT1L",
"gene_hgnc_id": 7623,
"hgvs_c": "c.345T>A",
"hgvs_p": "p.Asp115Glu",
"transcript": "NM_001329846.3",
"protein_id": "NP_001316775.1",
"transcript_support_level": null,
"aa_start": 115,
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"feature": null
},
{
"aa_ref": "D",
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"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYT1L",
"gene_hgnc_id": 7623,
"hgvs_c": "c.345T>A",
"hgvs_p": "p.Asp115Glu",
"transcript": "ENST00000647755.1",
"protein_id": "ENSP00000496922.1",
"transcript_support_level": null,
"aa_start": 115,
"aa_end": null,
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"cdna_start": 1040,
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"feature": null
},
{
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"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYT1L",
"gene_hgnc_id": 7623,
"hgvs_c": "c.345T>A",
"hgvs_p": "p.Asp115Glu",
"transcript": "NM_001329851.3",
"protein_id": "NP_001316780.1",
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"aa_start": 115,
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"aa_length": 1143,
"cds_start": 345,
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"cdna_start": 1174,
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"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYT1L",
"gene_hgnc_id": 7623,
"hgvs_c": "c.345T>A",
"hgvs_p": "p.Asp115Glu",
"transcript": "NM_001329852.3",
"protein_id": "NP_001316781.1",
"transcript_support_level": null,
"aa_start": 115,
"aa_end": null,
"aa_length": 1143,
"cds_start": 345,
"cds_end": null,
"cds_length": 3432,
"cdna_start": 1141,
"cdna_end": null,
"cdna_length": 7401,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYT1L",
"gene_hgnc_id": 7623,
"hgvs_c": "c.345T>A",
"hgvs_p": "p.Asp115Glu",
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}