Canonical Allele Identifier: CA1173064349

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259098C= , CM000663.2:g.67259098C=	GRCh38
NC_000001.10:g.67724781C= , CM000663.1:g.67724781C=	GRCh37
NC_000001.9:g.67497369C=	NCBI36
NG_011498.1:g.97613C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1699C=	ENSP00000513138.1:n.1699C=
ENST00000697150.1:c.1757C=	ENSP00000513139.1:n.1757C=
ENST00000697151.1:c.1690C=	ENSP00000513140.1:n.1690C=
ENST00000697164.1:c.1770C=	ENSP00000513153.1:p.His590=
ENST00000697165.1:c.1557C=	ENSP00000513154.1:p.His519=
ENST00000347310.10:c.1860C= MANE Select	ENSP00000321345.5:p.His620=
ENST00000637002.1:c.1251C=	ENSP00000490340.1:p.His417=
ENST00000347310.9:c.1860C=	ENSP00000321345.5:p.His620=
ENST00000395227.2:c.654C=	ENSP00000378652.2:p.His218=
ENST00000425614.3:c.1095C=	ENSP00000387640.2:p.His365=
ENST00000473881.2:c.*686C=	ENSP00000486667.1:n.*686C=
NM_144701.2:c.1860C=	NP_653302.2:p.His620=
XM_005270516.2:c.1098C=	XP_005270573.1:p.His366=
XM_011540789.1:c.1950C=	XP_011539091.1:p.His650=
XM_011540790.1:c.1860C=	XP_011539092.1:p.His620=
XM_011540791.1:c.1860C=	XP_011539093.1:p.His620=
XM_011540790.3:c.1860C=	XP_011539092.1:p.His620=
XM_011540791.3:c.1860C=	XP_011539093.1:p.His620=
XR_001736993.1:n.1940C=
NM_144701.3:c.1860C= MANE Select	NP_653302.2:p.His620=