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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: 17-47221774-G-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=17&pos=47221774&ref=G&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "17",
"pos": 47221774,
"ref": "G",
"alt": "A",
"effect": "missense_variant",
"transcript": "NM_002476.2",
"consequences": [
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYL4",
"gene_hgnc_id": 7585,
"hgvs_c": "c.406G>A",
"hgvs_p": "p.Val136Met",
"transcript": "NM_002476.2",
"protein_id": "NP_002467.1",
"transcript_support_level": null,
"aa_start": 136,
"aa_end": null,
"aa_length": 197,
"cds_start": 406,
"cds_end": null,
"cds_length": 594,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000393450.5",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_002476.2"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYL4",
"gene_hgnc_id": 7585,
"hgvs_c": "c.406G>A",
"hgvs_p": "p.Val136Met",
"transcript": "ENST00000393450.5",
"protein_id": "ENSP00000377096.1",
"transcript_support_level": 1,
"aa_start": 136,
"aa_end": null,
"aa_length": 197,
"cds_start": 406,
"cds_end": null,
"cds_length": 594,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_002476.2",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000393450.5"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYL4",
"gene_hgnc_id": 7585,
"hgvs_c": "c.406G>A",
"hgvs_p": "p.Val136Met",
"transcript": "ENST00000954741.1",
"protein_id": "ENSP00000624800.1",
"transcript_support_level": null,
"aa_start": 136,
"aa_end": null,
"aa_length": 215,
"cds_start": 406,
"cds_end": null,
"cds_length": 648,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000954741.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYL4",
"gene_hgnc_id": 7585,
"hgvs_c": "c.406G>A",
"hgvs_p": "p.Val136Met",
"transcript": "ENST00000954746.1",
"protein_id": "ENSP00000624805.1",
"transcript_support_level": null,
"aa_start": 136,
"aa_end": null,
"aa_length": 215,
"cds_start": 406,
"cds_end": null,
"cds_length": 648,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000954746.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYL4",
"gene_hgnc_id": 7585,
"hgvs_c": "c.406G>A",
"hgvs_p": "p.Val136Met",
"transcript": "ENST00000954750.1",
"protein_id": "ENSP00000624809.1",
"transcript_support_level": null,
"aa_start": 136,
"aa_end": null,
"aa_length": 215,
"cds_start": 406,
"cds_end": null,
"cds_length": 648,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000954750.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYL4",
"gene_hgnc_id": 7585,
"hgvs_c": "c.406G>A",
"hgvs_p": "p.Val136Met",
"transcript": "ENST00000954759.1",
"protein_id": "ENSP00000624818.1",
"transcript_support_level": null,
"aa_start": 136,
"aa_end": null,
"aa_length": 215,
"cds_start": 406,
"cds_end": null,
"cds_length": 648,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000954759.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYL4",
"gene_hgnc_id": 7585,
"hgvs_c": "c.406G>A",
"hgvs_p": "p.Val136Met",
"transcript": "NM_001002841.2",
"protein_id": "NP_001002841.1",
"transcript_support_level": null,
"aa_start": 136,
"aa_end": null,
"aa_length": 197,
"cds_start": 406,
"cds_end": null,
"cds_length": 594,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001002841.2"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYL4",
"gene_hgnc_id": 7585,
"hgvs_c": "c.406G>A",
"hgvs_p": "p.Val136Met",
"transcript": "ENST00000354968.5",
"protein_id": "ENSP00000347055.1",
"transcript_support_level": 5,
"aa_start": 136,
"aa_end": null,
"aa_length": 197,
"cds_start": 406,
"cds_end": null,
"cds_length": 594,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000354968.5"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYL4",
"gene_hgnc_id": 7585,
"hgvs_c": "c.406G>A",
"hgvs_p": "p.Val136Met",
"transcript": "ENST00000572316.5",
"protein_id": "ENSP00000461570.1",
"transcript_support_level": 5,
"aa_start": 136,
"aa_end": null,
"aa_length": 197,
"cds_start": 406,
"cds_end": null,
"cds_length": 594,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000572316.5"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYL4",
"gene_hgnc_id": 7585,
"hgvs_c": "c.406G>A",
"hgvs_p": "p.Val136Met",
"transcript": "ENST00000869091.1",
"protein_id": "ENSP00000539150.1",
"transcript_support_level": null,
"aa_start": 136,
"aa_end": null,
"aa_length": 197,
"cds_start": 406,
"cds_end": null,
"cds_length": 594,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000869091.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYL4",
"gene_hgnc_id": 7585,
"hgvs_c": "c.406G>A",
"hgvs_p": "p.Val136Met",
"transcript": "ENST00000954742.1",
"protein_id": "ENSP00000624801.1",
"transcript_support_level": null,
"aa_start": 136,
"aa_end": null,
"aa_length": 197,
"cds_start": 406,
"cds_end": null,
"cds_length": 594,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000954742.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYL4",
"gene_hgnc_id": 7585,
"hgvs_c": "c.406G>A",
"hgvs_p": "p.Val136Met",
"transcript": "ENST00000954745.1",
"protein_id": "ENSP00000624804.1",
"transcript_support_level": null,
"aa_start": 136,
"aa_end": null,
"aa_length": 197,
"cds_start": 406,
"cds_end": null,
"cds_length": 594,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000954745.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYL4",
"gene_hgnc_id": 7585,
"hgvs_c": "c.406G>A",
"hgvs_p": "p.Val136Met",
"transcript": "ENST00000954751.1",
"protein_id": "ENSP00000624810.1",
"transcript_support_level": null,
"aa_start": 136,
"aa_end": null,
"aa_length": 197,
"cds_start": 406,
"cds_end": null,
"cds_length": 594,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000954751.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYL4",
"gene_hgnc_id": 7585,
"hgvs_c": "c.406G>A",
"hgvs_p": "p.Val136Met",
"transcript": "ENST00000954752.1",
"protein_id": "ENSP00000624811.1",
"transcript_support_level": null,
"aa_start": 136,
"aa_end": null,
"aa_length": 197,
"cds_start": 406,
"cds_end": null,
"cds_length": 594,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000954752.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYL4",
"gene_hgnc_id": 7585,
"hgvs_c": "c.406G>A",
"hgvs_p": "p.Val136Met",
"transcript": "ENST00000954754.1",
"protein_id": "ENSP00000624813.1",
"transcript_support_level": null,
"aa_start": 136,
"aa_end": null,
"aa_length": 197,
"cds_start": 406,
"cds_end": null,
"cds_length": 594,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000954754.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYL4",
"gene_hgnc_id": 7585,
"hgvs_c": "c.406G>A",
"hgvs_p": "p.Val136Met",
"transcript": "ENST00000954755.1",
"protein_id": "ENSP00000624814.1",
"transcript_support_level": null,
"aa_start": 136,
"aa_end": null,
"aa_length": 197,
"cds_start": 406,
"cds_end": null,
"cds_length": 594,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000954755.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYL4",
"gene_hgnc_id": 7585,
"hgvs_c": "c.406G>A",
"hgvs_p": "p.Val136Met",
"transcript": "ENST00000954758.1",
"protein_id": "ENSP00000624817.1",
"transcript_support_level": null,
"aa_start": 136,
"aa_end": null,
"aa_length": 197,
"cds_start": 406,
"cds_end": null,
"cds_length": 594,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000954758.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYL4",
"gene_hgnc_id": 7585,
"hgvs_c": "c.406G>A",
"hgvs_p": "p.Val136Met",
"transcript": "ENST00000954743.1",
"protein_id": "ENSP00000624802.1",
"transcript_support_level": null,
"aa_start": 136,
"aa_end": null,
"aa_length": 196,
"cds_start": 406,
"cds_end": null,
"cds_length": 591,
"cdna_start": null,
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"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000954743.1"
},
{
"aa_ref": "V",
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"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
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],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYL4",
"gene_hgnc_id": 7585,
"hgvs_c": "c.406G>A",
"hgvs_p": "p.Val136Met",
"transcript": "ENST00000954747.1",
"protein_id": "ENSP00000624806.1",
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"aa_start": 136,
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"cds_end": null,
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"cdna_start": null,
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"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000954747.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYL4",
"gene_hgnc_id": 7585,
"hgvs_c": "c.406G>A",
"hgvs_p": "p.Val136Met",
"transcript": "ENST00000954748.1",
"protein_id": "ENSP00000624807.1",
"transcript_support_level": null,
"aa_start": 136,
"aa_end": null,
"aa_length": 196,
"cds_start": 406,
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"cdna_start": null,
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"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000954748.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYL4",
"gene_hgnc_id": 7585,
"hgvs_c": "c.406G>A",
"hgvs_p": "p.Val136Met",
"transcript": "ENST00000536623.6",
"protein_id": "ENSP00000442375.2",
"transcript_support_level": 5,
"aa_start": 136,
"aa_end": null,
"aa_length": 195,
"cds_start": 406,
"cds_end": null,
"cds_length": 590,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000536623.6"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYL4",
"gene_hgnc_id": 7585,
"hgvs_c": "c.400G>A",
"hgvs_p": "p.Val134Met",
"transcript": "ENST00000954756.1",
"protein_id": "ENSP00000624815.1",
"transcript_support_level": null,
"aa_start": 134,
"aa_end": null,
"aa_length": 194,
"cds_start": 400,
"cds_end": null,
"cds_length": 585,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000954756.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
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