Canonical Allele Identifier: CA2942698
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs774007183
ExAC: 4:69535870 G / A
gnomAD v2: 4-69535870-G-A
gnomAD v3: 4-68670152-G-A
gnomAD v4: 4-68670152-G-A
COSMIC: COSM3605126
MyVariant Identifiers: chr4:g.69535870G>A (hg19) chr4:g.68670152G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670152G>A , CM000666.2:g.68670152G>A GRCh38
NC_000004.11:g.69535870G>A , CM000666.1:g.69535870G>A GRCh37
NC_000004.10:g.69218465G>A NCBI36
NG_052676.1:g.5625C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.467C>T MANE Select ENSP00000341045.5:p.Pro156Leu
ENST00000338206.5:c.467C>T ENSP00000341045.5:p.Pro156Leu
ENST00000616841.4:c.467C>T ENSP00000482004.1:p.Pro156Leu
NM_001076.3:c.467C>T NP_001067.2:p.Pro156Leu
NM_001076.4:c.467C>T MANE Select NP_001067.2:p.Pro156Leu
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