Canonical Allele Identifier: CA1173064328

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259028G= , CM000663.2:g.67259028G=	GRCh38
NC_000001.10:g.67724711G= , CM000663.1:g.67724711G=	GRCh37
NC_000001.9:g.67497299G=	NCBI36
NG_011498.1:g.97543G=

Transcript Alleles

HGVS	Amino-acid Change
NM_144701.3:c.1790G= MANE Select	NP_653302.2:p.Cys597=
ENST00000347310.10:c.1790G= MANE Select	ENSP00000321345.5:p.Cys597=
NM_144701.2:c.1790G=	NP_653302.2:p.Cys597=
ENST00000347310.9:c.1790G=	ENSP00000321345.5:p.Cys597=
ENST00000395227.2:c.584G=	ENSP00000378652.2:p.Cys195=
ENST00000425614.3:c.1025G=	ENSP00000387640.2:p.Cys342=
ENST00000473881.2:c.*616G=	ENSP00000486667.1:n.*616G=
ENST00000637002.1:c.1181G=	ENSP00000490340.1:p.Cys394=
ENST00000697149.1:c.1629G=	ENSP00000513138.1:n.1629G=
ENST00000697150.1:c.1687G=	ENSP00000513139.1:n.1687G=
ENST00000697151.1:c.1620G=	ENSP00000513140.1:n.1620G=
ENST00000697164.1:c.1700G=	ENSP00000513153.1:p.Cys567=
ENST00000697165.1:c.1487G=	ENSP00000513154.1:p.Cys496=
XM_005270516.2:c.1028G=	XP_005270573.1:p.Cys343=
XM_011540789.1:c.1880G=	XP_011539091.1:p.Cys627=
XM_011540790.1:c.1790G=	XP_011539092.1:p.Cys597=
XM_011540790.3:c.1790G=	XP_011539092.1:p.Cys597=
XM_011540791.1:c.1790G=	XP_011539093.1:p.Cys597=
XM_011540791.3:c.1790G=	XP_011539093.1:p.Cys597=
XR_001736993.1:n.1870G=