Canonical Allele Identifier: CA1466050172

Gene: UGT2B7 UGT2B11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.69098371A= , CM000666.2:g.69098371A=	GRCh38
NC_000004.11:g.69964089A= , CM000666.1:g.69964089A=	GRCh37
NC_000004.10:g.69998678A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305231.12:c.722-169A= (UGT2B7) MANE Select	ENSP00000304811.7:n.722-169A=
ENST00000305231.11:c.722-169A= (UGT2B7)	ENSP00000304811.7:n.722-169A=
ENST00000502942.5:c.-26-169A= (UGT2B7)	ENSP00000426206.1:n.-26-169A=
ENST00000508661.5:c.722-169A= (UGT2B7)	ENSP00000427659.1:n.722-169A=
ENST00000509763.1:n.260-169A= (UGT2B7)
ENST00000615638.4:c.*106-93618T= (UGT2B11)	ENSP00000477842.1:n.*106-93618T=
ENST00000620779.4:c.*380-93618T= (UGT2B11)	ENSP00000478182.1:n.*380-93618T=
ENST00000622664.1:c.722-169A= (UGT2B7)	ENSP00000483172.1:n.722-169A=
NM_001074.2:c.722-169A= (UGT2B7)	NP_001065.2:n.722-169A=
XM_005265702.2:c.-26-169A= (UGT2B7)	XP_005265759.1:n.-26-169A=
XM_011532229.1:c.722-169A= (UGT2B7)	XP_011530531.1:n.722-169A=
XM_011532230.1:c.722-169A= (UGT2B7)	XP_011530532.1:n.722-169A=
XM_011532231.1:c.-26-169A= (UGT2B7)	XP_011530533.1:n.-26-169A=
NM_001074.3:c.722-169A= (UGT2B7)	NP_001065.2:n.722-169A=
NM_001330719.1:c.722-169A= (UGT2B7)	NP_001317648.1:n.722-169A=
NM_001349568.1:c.-26-169A= (UGT2B7)	NP_001336497.1:n.-26-169A=
XM_011532229.2:c.722-169A= (UGT2B7)	XP_011530531.1:n.722-169A=
NM_001074.4:c.722-169A= (UGT2B7) MANE Select	NP_001065.2:n.722-169A=
NM_001330719.2:c.722-169A= (UGT2B7)	NP_001317648.1:n.722-169A=
NM_001349568.2:c.-26-169A= (UGT2B7)	NP_001336497.1:n.-26-169A=