Canonical Allele Identifier: CA1465820713

Gene: UGT2B15

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68646658A= , CM000666.2:g.68646658A=	GRCh38
NC_000004.11:g.69512376A= , CM000666.1:g.69512376A=	GRCh37
NC_000004.10:g.69194971A=	NCBI36
NG_052676.1:g.29119T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338206.6:c.*446T= MANE Select	ENSP00000341045.5:n.*446T=
ENST00000338206.5:c.*446T=	ENSP00000341045.5:n.*446T=
ENST00000616841.4:c.1732+307T=	ENSP00000482004.1:n.1732+307T=
NM_001076.3:c.*446T=	NP_001067.2:n.*446T=
NM_001076.4:c.*446T= MANE Select	NP_001067.2:n.*446T=