Canonical Allele Identifier: CA1173064321

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259000A= , CM000663.2:g.67259000A=	GRCh38
NC_000001.10:g.67724683A= , CM000663.1:g.67724683A=	GRCh37
NC_000001.9:g.67497271A=	NCBI36
NG_011498.1:g.97515A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1601A=	ENSP00000513138.1:n.1601A=
ENST00000697150.1:c.1659A=	ENSP00000513139.1:n.1659A=
ENST00000697151.1:c.1592A=	ENSP00000513140.1:n.1592A=
ENST00000697164.1:c.1672A=	ENSP00000513153.1:p.Thr558=
ENST00000697165.1:c.1459A=	ENSP00000513154.1:p.Thr487=
ENST00000347310.10:c.1762A= MANE Select	ENSP00000321345.5:p.Thr588=
ENST00000637002.1:c.1153A=	ENSP00000490340.1:p.Thr385=
ENST00000347310.9:c.1762A=	ENSP00000321345.5:p.Thr588=
ENST00000395227.2:c.556A=	ENSP00000378652.2:p.Thr186=
ENST00000425614.3:c.997A=	ENSP00000387640.2:p.Thr333=
ENST00000473881.2:c.*588A=	ENSP00000486667.1:n.*588A=
NM_144701.2:c.1762A=	NP_653302.2:p.Thr588=
XM_005270516.2:c.1000A=	XP_005270573.1:p.Thr334=
XM_011540789.1:c.1852A=	XP_011539091.1:p.Thr618=
XM_011540790.1:c.1762A=	XP_011539092.1:p.Thr588=
XM_011540791.1:c.1762A=	XP_011539093.1:p.Thr588=
XM_011540790.3:c.1762A=	XP_011539092.1:p.Thr588=
XM_011540791.3:c.1762A=	XP_011539093.1:p.Thr588=
XR_001736993.1:n.1842A=
NM_144701.3:c.1762A= MANE Select	NP_653302.2:p.Thr588=