Canonical Allele Identifier: CA1173064311

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258980G= , CM000663.2:g.67258980G=	GRCh38
NC_000001.10:g.67724663G= , CM000663.1:g.67724663G=	GRCh37
NC_000001.9:g.67497251G=	NCBI36
NG_011498.1:g.97495G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1581G=	ENSP00000513138.1:n.1581G=
ENST00000697150.1:c.1639G=	ENSP00000513139.1:n.1639G=
ENST00000697151.1:c.1572G=	ENSP00000513140.1:n.1572G=
ENST00000697164.1:c.1652G=	ENSP00000513153.1:p.Ser551=
ENST00000697165.1:c.1439G=	ENSP00000513154.1:p.Ser480=
ENST00000347310.10:c.1742G= MANE Select	ENSP00000321345.5:p.Ser581=
ENST00000637002.1:c.1133G=	ENSP00000490340.1:p.Ser378=
ENST00000347310.9:c.1742G=	ENSP00000321345.5:p.Ser581=
ENST00000395227.2:c.536G=	ENSP00000378652.2:p.Ser179=
ENST00000425614.3:c.977G=	ENSP00000387640.2:p.Ser326=
ENST00000473881.2:c.*568G=	ENSP00000486667.1:n.*568G=
NM_144701.2:c.1742G=	NP_653302.2:p.Ser581=
XM_005270516.2:c.980G=	XP_005270573.1:p.Ser327=
XM_011540789.1:c.1832G=	XP_011539091.1:p.Ser611=
XM_011540790.1:c.1742G=	XP_011539092.1:p.Ser581=
XM_011540791.1:c.1742G=	XP_011539093.1:p.Ser581=
XM_011540790.3:c.1742G=	XP_011539092.1:p.Ser581=
XM_011540791.3:c.1742G=	XP_011539093.1:p.Ser581=
XR_001736993.1:n.1822G=
NM_144701.3:c.1742G= MANE Select	NP_653302.2:p.Ser581=