Canonical Allele Identifier: CA1465883959

Gene: UGT2B10

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68817128C= , CM000666.2:g.68817128C=	GRCh38
NC_000004.11:g.69682846C= , CM000666.1:g.69682846C=	GRCh37
NC_000004.10:g.69717435C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265403.12:c.718+391C= MANE Select	ENSP00000265403.7:n.718+391C=
ENST00000265403.11:c.718+391C=	ENSP00000265403.7:n.718+391C=
ENST00000458688.2:c.466+643C=	ENSP00000413420.2:n.466+643C=
NM_001075.5:c.718+391C=	NP_001066.1:n.718+391C=
NM_001144767.2:c.466+643C=	NP_001138239.1:n.466+643C=
NM_001290091.1:c.-26-901C=	NP_001277020.1:n.-26-901C=
XM_017008585.2:c.718+391C=	XP_016864074.1:n.718+391C=
NM_001075.6:c.718+391C= MANE Select	NP_001066.1:n.718+391C=
NM_001144767.3:c.466+643C=	NP_001138239.1:n.466+643C=
NM_001290091.2:c.-26-901C=	NP_001277020.1:n.-26-901C=