Canonical Allele Identifier: CA1173064341

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259068T= , CM000663.2:g.67259068T=	GRCh38
NC_000001.10:g.67724751T= , CM000663.1:g.67724751T=	GRCh37
NC_000001.9:g.67497339T=	NCBI36
NG_011498.1:g.97583T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1669T=	ENSP00000513138.1:n.1669T=
ENST00000697150.1:c.1727T=	ENSP00000513139.1:n.1727T=
ENST00000697151.1:c.1660T=	ENSP00000513140.1:n.1660T=
ENST00000697164.1:c.1740T=	ENSP00000513153.1:p.Thr580=
ENST00000697165.1:c.1527T=	ENSP00000513154.1:p.Thr509=
ENST00000347310.10:c.1830T= MANE Select	ENSP00000321345.5:p.Thr610=
ENST00000637002.1:c.1221T=	ENSP00000490340.1:p.Thr407=
ENST00000347310.9:c.1830T=	ENSP00000321345.5:p.Thr610=
ENST00000395227.2:c.624T=	ENSP00000378652.2:p.Thr208=
ENST00000425614.3:c.1065T=	ENSP00000387640.2:p.Thr355=
ENST00000473881.2:c.*656T=	ENSP00000486667.1:n.*656T=
NM_144701.2:c.1830T=	NP_653302.2:p.Thr610=
XM_005270516.2:c.1068T=	XP_005270573.1:p.Thr356=
XM_011540789.1:c.1920T=	XP_011539091.1:p.Thr640=
XM_011540790.1:c.1830T=	XP_011539092.1:p.Thr610=
XM_011540791.1:c.1830T=	XP_011539093.1:p.Thr610=
XM_011540790.3:c.1830T=	XP_011539092.1:p.Thr610=
XM_011540791.3:c.1830T=	XP_011539093.1:p.Thr610=
XR_001736993.1:n.1910T=
NM_144701.3:c.1830T= MANE Select	NP_653302.2:p.Thr610=