Canonical Allele Identifier: CA1173064256

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258760A= , CM000663.2:g.67258760A=	GRCh38
NC_000001.10:g.67724443A= , CM000663.1:g.67724443A=	GRCh37
NC_000001.9:g.67497031A=	NCBI36
NG_011498.1:g.97275A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1361A=	ENSP00000513138.1:n.1361A=
ENST00000697150.1:c.1419A=	ENSP00000513139.1:n.1419A=
ENST00000697151.1:c.1352A=	ENSP00000513140.1:n.1352A=
ENST00000697164.1:c.1432A=	ENSP00000513153.1:p.Thr478=
ENST00000697165.1:c.1219A=	ENSP00000513154.1:p.Thr407=
ENST00000347310.10:c.1522A= MANE Select	ENSP00000321345.5:p.Thr508=
ENST00000637002.1:c.913A=	ENSP00000490340.1:p.Thr305=
ENST00000347310.9:c.1522A=	ENSP00000321345.5:p.Thr508=
ENST00000395227.2:c.316A=	ENSP00000378652.2:p.Thr106=
ENST00000425614.3:c.757A=	ENSP00000387640.2:p.Thr253=
ENST00000473881.2:c.*348A=	ENSP00000486667.1:n.*348A=
NM_144701.2:c.1522A=	NP_653302.2:p.Thr508=
XM_005270516.2:c.760A=	XP_005270573.1:p.Thr254=
XM_011540789.1:c.1612A=	XP_011539091.1:p.Thr538=
XM_011540790.1:c.1522A=	XP_011539092.1:p.Thr508=
XM_011540791.1:c.1522A=	XP_011539093.1:p.Thr508=
XM_011540790.3:c.1522A=	XP_011539092.1:p.Thr508=
XM_011540791.3:c.1522A=	XP_011539093.1:p.Thr508=
XR_001736993.1:n.1602A=
NM_144701.3:c.1522A= MANE Select	NP_653302.2:p.Thr508=