Canonical Allele Identifier: CA1465883968

Gene: UGT2B10

Linked Data

• dbSNP Id: rs1737253897

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68817143C>T , CM000666.2:g.68817143C>T	GRCh38
NC_000004.11:g.69682861C>T , CM000666.1:g.69682861C>T	GRCh37
NC_000004.10:g.69717450C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265403.12:c.718+406C>T MANE Select	ENSP00000265403.7:n.718+406C>T
ENST00000265403.11:c.718+406C>T	ENSP00000265403.7:n.718+406C>T
ENST00000458688.2:c.466+658C>T	ENSP00000413420.2:n.466+658C>T
NM_001075.5:c.718+406C>T	NP_001066.1:n.718+406C>T
NM_001144767.2:c.466+658C>T	NP_001138239.1:n.466+658C>T
NM_001290091.1:c.-26-886C>T	NP_001277020.1:n.-26-886C>T
XM_017008585.2:c.718+406C>T	XP_016864074.1:n.718+406C>T
NM_001075.6:c.718+406C>T MANE Select	NP_001066.1:n.718+406C>T
NM_001144767.3:c.466+658C>T	NP_001138239.1:n.466+658C>T
NM_001290091.2:c.-26-886C>T	NP_001277020.1:n.-26-886C>T