Canonical Allele Identifier: CA1465820902

Gene: UGT2B15

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68646949T= , CM000666.2:g.68646949T=	GRCh38
NC_000004.11:g.69512667T= , CM000666.1:g.69512667T=	GRCh37
NC_000004.10:g.69195262T=	NCBI36
NG_052676.1:g.28828A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338206.6:c.*155A= MANE Select	ENSP00000341045.5:n.*155A=
ENST00000338206.5:c.*155A=	ENSP00000341045.5:n.*155A=
ENST00000616841.4:c.1732+16A=	ENSP00000482004.1:n.1732+16A=
NM_001076.3:c.*155A=	NP_001067.2:n.*155A=
NM_001076.4:c.*155A= MANE Select	NP_001067.2:n.*155A=