Canonical Allele Identifier: CA3081745139

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259118T= , CM000663.2:g.67259118T=	GRCh38
NC_000001.10:g.67724801T= , CM000663.1:g.67724801T=	GRCh37
NC_000001.9:g.67497389T=	NCBI36
NG_011498.1:g.97633T=

Transcript Alleles

HGVS	Amino-acid Change
NM_144701.3:c.1880T= MANE Select	NP_653302.2:p.Leu627=
ENST00000347310.10:c.1880T= MANE Select	ENSP00000321345.5:p.Leu627=
NM_144701.2:c.1880T=	NP_653302.2:p.Leu627=
ENST00000347310.9:c.1880T=	ENSP00000321345.5:p.Leu627=
ENST00000395227.2:c.674T=	ENSP00000378652.2:p.Leu225=
ENST00000425614.3:c.1115T=	ENSP00000387640.2:p.Leu372=
ENST00000473881.2:c.*706T=	ENSP00000486667.1:n.*706T=
ENST00000637002.1:c.1271T=	ENSP00000490340.1:p.Leu424=
ENST00000697149.1:c.1719T=	ENSP00000513138.1:n.1719T=
ENST00000697150.1:c.1777T=	ENSP00000513139.1:n.1777T=
ENST00000697151.1:c.1710T=	ENSP00000513140.1:n.1710T=
ENST00000697164.1:c.1790T=	ENSP00000513153.1:p.Leu597=
ENST00000697165.1:c.1577T=	ENSP00000513154.1:p.Leu526=
XM_005270516.2:c.1118T=	XP_005270573.1:p.Leu373=
XM_011540789.1:c.1970T=	XP_011539091.1:p.Leu657=
XM_011540790.1:c.1880T=	XP_011539092.1:p.Leu627=
XM_011540790.3:c.1880T=	XP_011539092.1:p.Leu627=
XM_011540791.1:c.1880T=	XP_011539093.1:p.Leu627=
XM_011540791.3:c.1880T=	XP_011539093.1:p.Leu627=
XR_001736993.1:n.1960T=