Canonical Allele Identifier: CA1143430079

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259097A= , CM000663.2:g.67259097A=	GRCh38
NC_000001.10:g.67724780A= , CM000663.1:g.67724780A=	GRCh37
NC_000001.9:g.67497368A=	NCBI36
NG_011498.1:g.97612A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1698A=	ENSP00000513138.1:n.1698A=
ENST00000697150.1:c.1756A=	ENSP00000513139.1:n.1756A=
ENST00000697151.1:c.1689A=	ENSP00000513140.1:n.1689A=
ENST00000697164.1:c.1769A=	ENSP00000513153.1:p.His590=
ENST00000697165.1:c.1556A=	ENSP00000513154.1:p.His519=
ENST00000347310.10:c.1859A= MANE Select	ENSP00000321345.5:p.His620=
ENST00000637002.1:c.1250A=	ENSP00000490340.1:p.His417=
ENST00000347310.9:c.1859A=	ENSP00000321345.5:p.His620=
ENST00000395227.2:c.653A=	ENSP00000378652.2:p.His218=
ENST00000425614.3:c.1094A=	ENSP00000387640.2:p.His365=
ENST00000473881.2:c.*685A=	ENSP00000486667.1:n.*685A=
NM_144701.2:c.1859A=	NP_653302.2:p.His620=
XM_005270516.2:c.1097A=	XP_005270573.1:p.His366=
XM_011540789.1:c.1949A=	XP_011539091.1:p.His650=
XM_011540790.1:c.1859A=	XP_011539092.1:p.His620=
XM_011540791.1:c.1859A=	XP_011539093.1:p.His620=
XM_011540790.3:c.1859A=	XP_011539092.1:p.His620=
XM_011540791.3:c.1859A=	XP_011539093.1:p.His620=
XR_001736993.1:n.1939A=
NM_144701.3:c.1859A= MANE Select	NP_653302.2:p.His620=