Canonical Allele Identifier: CA1173064285

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258880G= , CM000663.2:g.67258880G=	GRCh38
NC_000001.10:g.67724563G= , CM000663.1:g.67724563G=	GRCh37
NC_000001.9:g.67497151G=	NCBI36
NG_011498.1:g.97395G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1481G=	ENSP00000513138.1:n.1481G=
ENST00000697150.1:c.1539G=	ENSP00000513139.1:n.1539G=
ENST00000697151.1:c.1472G=	ENSP00000513140.1:n.1472G=
ENST00000697164.1:c.1552G=	ENSP00000513153.1:p.Glu518=
ENST00000697165.1:c.1339G=	ENSP00000513154.1:p.Glu447=
ENST00000347310.10:c.1642G= MANE Select	ENSP00000321345.5:p.Glu548=
ENST00000637002.1:c.1033G=	ENSP00000490340.1:p.Glu345=
ENST00000347310.9:c.1642G=	ENSP00000321345.5:p.Glu548=
ENST00000395227.2:c.436G=	ENSP00000378652.2:p.Glu146=
ENST00000425614.3:c.877G=	ENSP00000387640.2:p.Glu293=
ENST00000473881.2:c.*468G=	ENSP00000486667.1:n.*468G=
NM_144701.2:c.1642G=	NP_653302.2:p.Glu548=
XM_005270516.2:c.880G=	XP_005270573.1:p.Glu294=
XM_011540789.1:c.1732G=	XP_011539091.1:p.Glu578=
XM_011540790.1:c.1642G=	XP_011539092.1:p.Glu548=
XM_011540791.1:c.1642G=	XP_011539093.1:p.Glu548=
XM_011540790.3:c.1642G=	XP_011539092.1:p.Glu548=
XM_011540791.3:c.1642G=	XP_011539093.1:p.Glu548=
XR_001736993.1:n.1722G=
NM_144701.3:c.1642G= MANE Select	NP_653302.2:p.Glu548=