Canonical Allele Identifier: CA1173064303

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258941A= , CM000663.2:g.67258941A=	GRCh38
NC_000001.10:g.67724624A= , CM000663.1:g.67724624A=	GRCh37
NC_000001.9:g.67497212A=	NCBI36
NG_011498.1:g.97456A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1542A=	ENSP00000513138.1:n.1542A=
ENST00000697150.1:c.1600A=	ENSP00000513139.1:n.1600A=
ENST00000697151.1:c.1533A=	ENSP00000513140.1:n.1533A=
ENST00000697164.1:c.1613A=	ENSP00000513153.1:p.Glu538=
ENST00000697165.1:c.1400A=	ENSP00000513154.1:p.Glu467=
ENST00000347310.10:c.1703A= MANE Select	ENSP00000321345.5:p.Glu568=
ENST00000637002.1:c.1094A=	ENSP00000490340.1:p.Glu365=
ENST00000347310.9:c.1703A=	ENSP00000321345.5:p.Glu568=
ENST00000395227.2:c.497A=	ENSP00000378652.2:p.Glu166=
ENST00000425614.3:c.938A=	ENSP00000387640.2:p.Glu313=
ENST00000473881.2:c.*529A=	ENSP00000486667.1:n.*529A=
NM_144701.2:c.1703A=	NP_653302.2:p.Glu568=
XM_005270516.2:c.941A=	XP_005270573.1:p.Glu314=
XM_011540789.1:c.1793A=	XP_011539091.1:p.Glu598=
XM_011540790.1:c.1703A=	XP_011539092.1:p.Glu568=
XM_011540791.1:c.1703A=	XP_011539093.1:p.Glu568=
XM_011540790.3:c.1703A=	XP_011539092.1:p.Glu568=
XM_011540791.3:c.1703A=	XP_011539093.1:p.Glu568=
XR_001736993.1:n.1783A=
NM_144701.3:c.1703A= MANE Select	NP_653302.2:p.Glu568=