Canonical Allele Identifier: CA357090197

Gene: UGT2B10

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68822269A>T , CM000666.2:g.68822269A>T	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
NM_001075.6:c.868-2A>T MANE Select	NP_001066.1:n.868-2A>T
ENST00000265403.12:c.868-2A>T MANE Select	ENSP00000265403.7:n.868-2A>T
NM_001075.5:c.868-2A>T	NP_001066.1:n.868-2A>T
NM_001144767.2:c.616-2A>T	NP_001138239.1:n.616-2A>T
NM_001144767.3:c.616-2A>T	NP_001138239.1:n.616-2A>T
NM_001290091.1:c.124-2A>T	NP_001277020.1:n.124-2A>T
NM_001290091.2:c.124-2A>T	NP_001277020.1:n.124-2A>T
ENST00000265403.11:c.868-2A>T	ENSP00000265403.7:n.868-2A>T
ENST00000458688.2:c.616-2A>T	ENSP00000413420.2:n.616-2A>T
XM_017008585.2:c.868-11A>T	XP_016864074.1:n.868-11A>T