Canonical Allele Identifier: CA1173064334

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259050G= , CM000663.2:g.67259050G=	GRCh38
NC_000001.10:g.67724733G= , CM000663.1:g.67724733G=	GRCh37
NC_000001.9:g.67497321G=	NCBI36
NG_011498.1:g.97565G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1651G=	ENSP00000513138.1:n.1651G=
ENST00000697150.1:c.1709G=	ENSP00000513139.1:n.1709G=
ENST00000697151.1:c.1642G=	ENSP00000513140.1:n.1642G=
ENST00000697164.1:c.1722G=	ENSP00000513153.1:p.Glu574=
ENST00000697165.1:c.1509G=	ENSP00000513154.1:p.Glu503=
ENST00000347310.10:c.1812G= MANE Select	ENSP00000321345.5:p.Glu604=
ENST00000637002.1:c.1203G=	ENSP00000490340.1:p.Glu401=
ENST00000347310.9:c.1812G=	ENSP00000321345.5:p.Glu604=
ENST00000395227.2:c.606G=	ENSP00000378652.2:p.Glu202=
ENST00000425614.3:c.1047G=	ENSP00000387640.2:p.Glu349=
ENST00000473881.2:c.*638G=	ENSP00000486667.1:n.*638G=
NM_144701.2:c.1812G=	NP_653302.2:p.Glu604=
XM_005270516.2:c.1050G=	XP_005270573.1:p.Glu350=
XM_011540789.1:c.1902G=	XP_011539091.1:p.Glu634=
XM_011540790.1:c.1812G=	XP_011539092.1:p.Glu604=
XM_011540791.1:c.1812G=	XP_011539093.1:p.Glu604=
XM_011540790.3:c.1812G=	XP_011539092.1:p.Glu604=
XM_011540791.3:c.1812G=	XP_011539093.1:p.Glu604=
XR_001736993.1:n.1892G=
NM_144701.3:c.1812G= MANE Select	NP_653302.2:p.Glu604=