Canonical Allele Identifier: CA1465894982

Gene: UGT2B10

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68830733A= , CM000666.2:g.68830733A=	GRCh38
NC_000004.11:g.69696451A= , CM000666.1:g.69696451A=	GRCh37
NC_000004.10:g.69731040A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265403.12:c.1441A= MANE Select	ENSP00000265403.7:p.Asn481=
ENST00000265403.11:c.1441A=	ENSP00000265403.7:p.Asn481=
ENST00000458688.2:c.1189A=	ENSP00000413420.2:p.Asn397=
NM_001075.5:c.1441A=	NP_001066.1:p.Asn481=
NM_001144767.2:c.1189A=	NP_001138239.1:p.Asn397=
NM_001290091.1:c.697A=	NP_001277020.1:p.Asn233=
XM_017008585.2:c.1432A=	XP_016864074.1:p.Asn478=
NM_001075.6:c.1441A= MANE Select	NP_001066.1:p.Asn481=
NM_001144767.3:c.1189A=	NP_001138239.1:p.Asn397=
NM_001290091.2:c.697A=	NP_001277020.1:p.Asn233=