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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: 7-1936765-C-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=7&pos=1936765&ref=C&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "7",
"pos": 1936765,
"ref": "C",
"alt": "A",
"effect": "missense_variant",
"transcript": "NM_003550.3",
"consequences": [
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MAD1L1",
"gene_hgnc_id": 6762,
"hgvs_c": "c.1729G>T",
"hgvs_p": "p.Ala577Ser",
"transcript": "NM_001013836.2",
"protein_id": "NP_001013858.1",
"transcript_support_level": null,
"aa_start": 577,
"aa_end": null,
"aa_length": 718,
"cds_start": 1729,
"cds_end": null,
"cds_length": 2157,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000265854.12",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001013836.2"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MAD1L1",
"gene_hgnc_id": 6762,
"hgvs_c": "c.1729G>T",
"hgvs_p": "p.Ala577Ser",
"transcript": "ENST00000265854.12",
"protein_id": "ENSP00000265854.7",
"transcript_support_level": 1,
"aa_start": 577,
"aa_end": null,
"aa_length": 718,
"cds_start": 1729,
"cds_end": null,
"cds_length": 2157,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_001013836.2",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000265854.12"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MAD1L1",
"gene_hgnc_id": 6762,
"hgvs_c": "c.1729G>T",
"hgvs_p": "p.Ala577Ser",
"transcript": "ENST00000406869.5",
"protein_id": "ENSP00000385334.1",
"transcript_support_level": 1,
"aa_start": 577,
"aa_end": null,
"aa_length": 718,
"cds_start": 1729,
"cds_end": null,
"cds_length": 2157,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000406869.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": true,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 22,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ENSG00000286192",
"gene_hgnc_id": null,
"hgvs_c": "n.*4489G>T",
"hgvs_p": null,
"transcript": "ENST00000651235.1",
"protein_id": "ENSP00000498895.1",
"transcript_support_level": null,
"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": null,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000651235.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": true,
"protein_coding": false,
"strand": false,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 22,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ENSG00000286192",
"gene_hgnc_id": null,
"hgvs_c": "n.*4489G>T",
"hgvs_p": null,
"transcript": "ENST00000651235.1",
"protein_id": "ENSP00000498895.1",
"transcript_support_level": null,
"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": null,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000651235.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MAD1L1",
"gene_hgnc_id": 6762,
"hgvs_c": "c.1798G>T",
"hgvs_p": "p.Ala600Ser",
"transcript": "ENST00000853805.1",
"protein_id": "ENSP00000523864.1",
"transcript_support_level": null,
"aa_start": 600,
"aa_end": null,
"aa_length": 741,
"cds_start": 1798,
"cds_end": null,
"cds_length": 2226,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000853805.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MAD1L1",
"gene_hgnc_id": 6762,
"hgvs_c": "c.1780G>T",
"hgvs_p": "p.Ala594Ser",
"transcript": "ENST00000853807.1",
"protein_id": "ENSP00000523866.1",
"transcript_support_level": null,
"aa_start": 594,
"aa_end": null,
"aa_length": 735,
"cds_start": 1780,
"cds_end": null,
"cds_length": 2208,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000853807.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MAD1L1",
"gene_hgnc_id": 6762,
"hgvs_c": "c.1729G>T",
"hgvs_p": "p.Ala577Ser",
"transcript": "NM_001013837.2",
"protein_id": "NP_001013859.1",
"transcript_support_level": null,
"aa_start": 577,
"aa_end": null,
"aa_length": 718,
"cds_start": 1729,
"cds_end": null,
"cds_length": 2157,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001013837.2"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MAD1L1",
"gene_hgnc_id": 6762,
"hgvs_c": "c.1729G>T",
"hgvs_p": "p.Ala577Ser",
"transcript": "NM_001304523.2",
"protein_id": "NP_001291452.1",
"transcript_support_level": null,
"aa_start": 577,
"aa_end": null,
"aa_length": 718,
"cds_start": 1729,
"cds_end": null,
"cds_length": 2157,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001304523.2"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MAD1L1",
"gene_hgnc_id": 6762,
"hgvs_c": "c.1729G>T",
"hgvs_p": "p.Ala577Ser",
"transcript": "NM_003550.3",
"protein_id": "NP_003541.2",
"transcript_support_level": null,
"aa_start": 577,
"aa_end": null,
"aa_length": 718,
"cds_start": 1729,
"cds_end": null,
"cds_length": 2157,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_003550.3"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MAD1L1",
"gene_hgnc_id": 6762,
"hgvs_c": "c.1729G>T",
"hgvs_p": "p.Ala577Ser",
"transcript": "ENST00000399654.6",
"protein_id": "ENSP00000382562.2",
"transcript_support_level": 5,
"aa_start": 577,
"aa_end": null,
"aa_length": 718,
"cds_start": 1729,
"cds_end": null,
"cds_length": 2157,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000399654.6"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MAD1L1",
"gene_hgnc_id": 6762,
"hgvs_c": "c.1729G>T",
"hgvs_p": "p.Ala577Ser",
"transcript": "ENST00000853791.1",
"protein_id": "ENSP00000523850.1",
"transcript_support_level": null,
"aa_start": 577,
"aa_end": null,
"aa_length": 718,
"cds_start": 1729,
"cds_end": null,
"cds_length": 2157,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000853791.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MAD1L1",
"gene_hgnc_id": 6762,
"hgvs_c": "c.1729G>T",
"hgvs_p": "p.Ala577Ser",
"transcript": "ENST00000853792.1",
"protein_id": "ENSP00000523851.1",
"transcript_support_level": null,
"aa_start": 577,
"aa_end": null,
"aa_length": 718,
"cds_start": 1729,
"cds_end": null,
"cds_length": 2157,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000853792.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MAD1L1",
"gene_hgnc_id": 6762,
"hgvs_c": "c.1729G>T",
"hgvs_p": "p.Ala577Ser",
"transcript": "ENST00000853796.1",
"protein_id": "ENSP00000523855.1",
"transcript_support_level": null,
"aa_start": 577,
"aa_end": null,
"aa_length": 718,
"cds_start": 1729,
"cds_end": null,
"cds_length": 2157,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000853796.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MAD1L1",
"gene_hgnc_id": 6762,
"hgvs_c": "c.1729G>T",
"hgvs_p": "p.Ala577Ser",
"transcript": "ENST00000853798.1",
"protein_id": "ENSP00000523857.1",
"transcript_support_level": null,
"aa_start": 577,
"aa_end": null,
"aa_length": 718,
"cds_start": 1729,
"cds_end": null,
"cds_length": 2157,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000853798.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MAD1L1",
"gene_hgnc_id": 6762,
"hgvs_c": "c.1729G>T",
"hgvs_p": "p.Ala577Ser",
"transcript": "ENST00000853799.1",
"protein_id": "ENSP00000523858.1",
"transcript_support_level": null,
"aa_start": 577,
"aa_end": null,
"aa_length": 718,
"cds_start": 1729,
"cds_end": null,
"cds_length": 2157,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000853799.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MAD1L1",
"gene_hgnc_id": 6762,
"hgvs_c": "c.1729G>T",
"hgvs_p": "p.Ala577Ser",
"transcript": "ENST00000853800.1",
"protein_id": "ENSP00000523859.1",
"transcript_support_level": null,
"aa_start": 577,
"aa_end": null,
"aa_length": 718,
"cds_start": 1729,
"cds_end": null,
"cds_length": 2157,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000853800.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MAD1L1",
"gene_hgnc_id": 6762,
"hgvs_c": "c.1729G>T",
"hgvs_p": "p.Ala577Ser",
"transcript": "ENST00000853803.1",
"protein_id": "ENSP00000523862.1",
"transcript_support_level": null,
"aa_start": 577,
"aa_end": null,
"aa_length": 718,
"cds_start": 1729,
"cds_end": null,
"cds_length": 2157,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000853803.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MAD1L1",
"gene_hgnc_id": 6762,
"hgvs_c": "c.1729G>T",
"hgvs_p": "p.Ala577Ser",
"transcript": "ENST00000967144.1",
"protein_id": "ENSP00000637203.1",
"transcript_support_level": null,
"aa_start": 577,
"aa_end": null,
"aa_length": 718,
"cds_start": 1729,
"cds_end": null,
"cds_length": 2157,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000967144.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MAD1L1",
"gene_hgnc_id": 6762,
"hgvs_c": "c.1729G>T",
"hgvs_p": "p.Ala577Ser",
"transcript": "ENST00000967148.1",
"protein_id": "ENSP00000637207.1",
"transcript_support_level": null,
"aa_start": 577,
"aa_end": null,
"aa_length": 718,
"cds_start": 1729,
"cds_end": null,
"cds_length": 2157,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000967148.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MAD1L1",
"gene_hgnc_id": 6762,
"hgvs_c": "c.1729G>T",
"hgvs_p": "p.Ala577Ser",
"transcript": "ENST00000967149.1",
"protein_id": "ENSP00000637208.1",
"transcript_support_level": null,
"aa_start": 577,
"aa_end": null,
"aa_length": 718,
"cds_start": 1729,
"cds_end": null,
"cds_length": 2157,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000967149.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MAD1L1",
"gene_hgnc_id": 6762,
"hgvs_c": "c.1672G>T",
"hgvs_p": "p.Ala558Ser",
"transcript": "ENST00000853793.1",
"protein_id": "ENSP00000523852.1",
"transcript_support_level": null,
"aa_start": 558,
"aa_end": null,
"aa_length": 699,
"cds_start": 1672,
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}
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}