Canonical Allele Identifier: CA1465883991

Gene: UGT2B10

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68817177A= , CM000666.2:g.68817177A=	GRCh38
NC_000004.11:g.69682895A= , CM000666.1:g.69682895A=	GRCh37
NC_000004.10:g.69717484A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265403.12:c.718+440A= MANE Select	ENSP00000265403.7:n.718+440A=
ENST00000265403.11:c.718+440A=	ENSP00000265403.7:n.718+440A=
ENST00000458688.2:c.466+692A=	ENSP00000413420.2:n.466+692A=
NM_001075.5:c.718+440A=	NP_001066.1:n.718+440A=
NM_001144767.2:c.466+692A=	NP_001138239.1:n.466+692A=
NM_001290091.1:c.-26-852A=	NP_001277020.1:n.-26-852A=
XM_017008585.2:c.718+440A=	XP_016864074.1:n.718+440A=
NM_001075.6:c.718+440A= MANE Select	NP_001066.1:n.718+440A=
NM_001144767.3:c.466+692A=	NP_001138239.1:n.466+692A=
NM_001290091.2:c.-26-852A=	NP_001277020.1:n.-26-852A=