Canonical Allele Identifier: CA1173064247

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258734G= , CM000663.2:g.67258734G=	GRCh38
NC_000001.10:g.67724417G= , CM000663.1:g.67724417G=	GRCh37
NC_000001.9:g.67497005G=	NCBI36
NG_011498.1:g.97249G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1335G=	ENSP00000513138.1:n.1335G=
ENST00000697150.1:c.1393G=	ENSP00000513139.1:n.1393G=
ENST00000697151.1:c.1326G=	ENSP00000513140.1:n.1326G=
ENST00000697164.1:c.1406G=	ENSP00000513153.1:p.Ser469=
ENST00000697165.1:c.1193G=	ENSP00000513154.1:p.Ser398=
ENST00000347310.10:c.1496G= MANE Select	ENSP00000321345.5:p.Ser499=
ENST00000637002.1:c.887G=	ENSP00000490340.1:p.Ser296=
ENST00000347310.9:c.1496G=	ENSP00000321345.5:p.Ser499=
ENST00000395227.2:c.290G=	ENSP00000378652.2:p.Ser97=
ENST00000425614.3:c.731G=	ENSP00000387640.2:p.Ser244=
ENST00000473881.2:c.*322G=	ENSP00000486667.1:n.*322G=
NM_144701.2:c.1496G=	NP_653302.2:p.Ser499=
XM_005270516.2:c.734G=	XP_005270573.1:p.Ser245=
XM_011540789.1:c.1586G=	XP_011539091.1:p.Ser529=
XM_011540790.1:c.1496G=	XP_011539092.1:p.Ser499=
XM_011540791.1:c.1496G=	XP_011539093.1:p.Ser499=
XM_011540790.3:c.1496G=	XP_011539092.1:p.Ser499=
XM_011540791.3:c.1496G=	XP_011539093.1:p.Ser499=
XR_001736993.1:n.1576G=
NM_144701.3:c.1496G= MANE Select	NP_653302.2:p.Ser499=