Canonical Allele Identifier: CA1173064331

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259037T= , CM000663.2:g.67259037T=	GRCh38
NC_000001.10:g.67724720T= , CM000663.1:g.67724720T=	GRCh37
NC_000001.9:g.67497308T=	NCBI36
NG_011498.1:g.97552T=

Transcript Alleles

HGVS	Amino-acid Change
NM_144701.3:c.1799T= MANE Select	NP_653302.2:p.Ile600=
ENST00000347310.10:c.1799T= MANE Select	ENSP00000321345.5:p.Ile600=
NM_144701.2:c.1799T=	NP_653302.2:p.Ile600=
ENST00000347310.9:c.1799T=	ENSP00000321345.5:p.Ile600=
ENST00000395227.2:c.593T=	ENSP00000378652.2:p.Ile198=
ENST00000425614.3:c.1034T=	ENSP00000387640.2:p.Ile345=
ENST00000473881.2:c.*625T=	ENSP00000486667.1:n.*625T=
ENST00000637002.1:c.1190T=	ENSP00000490340.1:p.Ile397=
ENST00000697149.1:c.1638T=	ENSP00000513138.1:n.1638T=
ENST00000697150.1:c.1696T=	ENSP00000513139.1:n.1696T=
ENST00000697151.1:c.1629T=	ENSP00000513140.1:n.1629T=
ENST00000697164.1:c.1709T=	ENSP00000513153.1:p.Ile570=
ENST00000697165.1:c.1496T=	ENSP00000513154.1:p.Ile499=
XM_005270516.2:c.1037T=	XP_005270573.1:p.Ile346=
XM_011540789.1:c.1889T=	XP_011539091.1:p.Ile630=
XM_011540790.1:c.1799T=	XP_011539092.1:p.Ile600=
XM_011540790.3:c.1799T=	XP_011539092.1:p.Ile600=
XM_011540791.1:c.1799T=	XP_011539093.1:p.Ile600=
XM_011540791.3:c.1799T=	XP_011539093.1:p.Ile600=
XR_001736993.1:n.1879T=