Canonical Allele Identifier: CA1465883729

Gene: UGT2B10

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68816784T= , CM000666.2:g.68816784T=	GRCh38
NC_000004.11:g.69682502T= , CM000666.1:g.69682502T=	GRCh37
NC_000004.10:g.69717091T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265403.12:c.718+47T= MANE Select	ENSP00000265403.7:n.718+47T=
ENST00000265403.11:c.718+47T=	ENSP00000265403.7:n.718+47T=
ENST00000458688.2:c.466+299T=	ENSP00000413420.2:n.466+299T=
NM_001075.5:c.718+47T=	NP_001066.1:n.718+47T=
NM_001144767.2:c.466+299T=	NP_001138239.1:n.466+299T=
NM_001290091.1:c.-27+612T=	NP_001277020.1:n.-27+612T=
XM_017008585.2:c.718+47T=	XP_016864074.1:n.718+47T=
NM_001075.6:c.718+47T= MANE Select	NP_001066.1:n.718+47T=
NM_001144767.3:c.466+299T=	NP_001138239.1:n.466+299T=
NM_001290091.2:c.-27+612T=	NP_001277020.1:n.-27+612T=