Canonical Allele Identifier: CA3081745077

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259046A= , CM000663.2:g.67259046A=	GRCh38
NC_000001.10:g.67724729A= , CM000663.1:g.67724729A=	GRCh37
NC_000001.9:g.67497317A=	NCBI36
NG_011498.1:g.97561A=

Transcript Alleles

HGVS	Amino-acid Change
NM_144701.3:c.1808A= MANE Select	NP_653302.2:p.Glu603=
ENST00000347310.10:c.1808A= MANE Select	ENSP00000321345.5:p.Glu603=
NM_144701.2:c.1808A=	NP_653302.2:p.Glu603=
ENST00000347310.9:c.1808A=	ENSP00000321345.5:p.Glu603=
ENST00000395227.2:c.602A=	ENSP00000378652.2:p.Glu201=
ENST00000425614.3:c.1043A=	ENSP00000387640.2:p.Glu348=
ENST00000473881.2:c.*634A=	ENSP00000486667.1:n.*634A=
ENST00000637002.1:c.1199A=	ENSP00000490340.1:p.Glu400=
ENST00000697149.1:c.1647A=	ENSP00000513138.1:n.1647A=
ENST00000697150.1:c.1705A=	ENSP00000513139.1:n.1705A=
ENST00000697151.1:c.1638A=	ENSP00000513140.1:n.1638A=
ENST00000697164.1:c.1718A=	ENSP00000513153.1:p.Glu573=
ENST00000697165.1:c.1505A=	ENSP00000513154.1:p.Glu502=
XM_005270516.2:c.1046A=	XP_005270573.1:p.Glu349=
XM_011540789.1:c.1898A=	XP_011539091.1:p.Glu633=
XM_011540790.1:c.1808A=	XP_011539092.1:p.Glu603=
XM_011540790.3:c.1808A=	XP_011539092.1:p.Glu603=
XM_011540791.1:c.1808A=	XP_011539093.1:p.Glu603=
XM_011540791.3:c.1808A=	XP_011539093.1:p.Glu603=
XR_001736993.1:n.1888A=