Canonical Allele Identifier: CA1173064266

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258806G= , CM000663.2:g.67258806G=	GRCh38
NC_000001.10:g.67724489G= , CM000663.1:g.67724489G=	GRCh37
NC_000001.9:g.67497077G=	NCBI36
NG_011498.1:g.97321G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1407G=	ENSP00000513138.1:n.1407G=
ENST00000697150.1:c.1465G=	ENSP00000513139.1:n.1465G=
ENST00000697151.1:c.1398G=	ENSP00000513140.1:n.1398G=
ENST00000697164.1:c.1478G=	ENSP00000513153.1:p.Arg493=
ENST00000697165.1:c.1265G=	ENSP00000513154.1:p.Arg422=
ENST00000347310.10:c.1568G= MANE Select	ENSP00000321345.5:p.Arg523=
ENST00000637002.1:c.959G=	ENSP00000490340.1:p.Arg320=
ENST00000347310.9:c.1568G=	ENSP00000321345.5:p.Arg523=
ENST00000395227.2:c.362G=	ENSP00000378652.2:p.Arg121=
ENST00000425614.3:c.803G=	ENSP00000387640.2:p.Arg268=
ENST00000473881.2:c.*394G=	ENSP00000486667.1:n.*394G=
NM_144701.2:c.1568G=	NP_653302.2:p.Arg523=
XM_005270516.2:c.806G=	XP_005270573.1:p.Arg269=
XM_011540789.1:c.1658G=	XP_011539091.1:p.Arg553=
XM_011540790.1:c.1568G=	XP_011539092.1:p.Arg523=
XM_011540791.1:c.1568G=	XP_011539093.1:p.Arg523=
XM_011540790.3:c.1568G=	XP_011539092.1:p.Arg523=
XM_011540791.3:c.1568G=	XP_011539093.1:p.Arg523=
XR_001736993.1:n.1648G=
NM_144701.3:c.1568G= MANE Select	NP_653302.2:p.Arg523=