Canonical Allele Identifier: CA3081745030

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259027T= , CM000663.2:g.67259027T=	GRCh38
NC_000001.10:g.67724710T= , CM000663.1:g.67724710T=	GRCh37
NC_000001.9:g.67497298T=	NCBI36
NG_011498.1:g.97542T=

Transcript Alleles

HGVS	Amino-acid Change
NM_144701.3:c.1789T= MANE Select	NP_653302.2:p.Cys597=
ENST00000347310.10:c.1789T= MANE Select	ENSP00000321345.5:p.Cys597=
NM_144701.2:c.1789T=	NP_653302.2:p.Cys597=
ENST00000347310.9:c.1789T=	ENSP00000321345.5:p.Cys597=
ENST00000395227.2:c.583T=	ENSP00000378652.2:p.Cys195=
ENST00000425614.3:c.1024T=	ENSP00000387640.2:p.Cys342=
ENST00000473881.2:c.*615T=	ENSP00000486667.1:n.*615T=
ENST00000637002.1:c.1180T=	ENSP00000490340.1:p.Cys394=
ENST00000697149.1:c.1628T=	ENSP00000513138.1:n.1628T=
ENST00000697150.1:c.1686T=	ENSP00000513139.1:n.1686T=
ENST00000697151.1:c.1619T=	ENSP00000513140.1:n.1619T=
ENST00000697164.1:c.1699T=	ENSP00000513153.1:p.Cys567=
ENST00000697165.1:c.1486T=	ENSP00000513154.1:p.Cys496=
XM_005270516.2:c.1027T=	XP_005270573.1:p.Cys343=
XM_011540789.1:c.1879T=	XP_011539091.1:p.Cys627=
XM_011540790.1:c.1789T=	XP_011539092.1:p.Cys597=
XM_011540790.3:c.1789T=	XP_011539092.1:p.Cys597=
XM_011540791.1:c.1789T=	XP_011539093.1:p.Cys597=
XM_011540791.3:c.1789T=	XP_011539093.1:p.Cys597=
XR_001736993.1:n.1869T=