Canonical Allele Identifier: CA1173064326

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259019T= , CM000663.2:g.67259019T=	GRCh38
NC_000001.10:g.67724702T= , CM000663.1:g.67724702T=	GRCh37
NC_000001.9:g.67497290T=	NCBI36
NG_011498.1:g.97534T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1620T=	ENSP00000513138.1:n.1620T=
ENST00000697150.1:c.1678T=	ENSP00000513139.1:n.1678T=
ENST00000697151.1:c.1611T=	ENSP00000513140.1:n.1611T=
ENST00000697164.1:c.1691T=	ENSP00000513153.1:p.Phe564=
ENST00000697165.1:c.1478T=	ENSP00000513154.1:p.Phe493=
ENST00000347310.10:c.1781T= MANE Select	ENSP00000321345.5:p.Phe594=
ENST00000637002.1:c.1172T=	ENSP00000490340.1:p.Phe391=
ENST00000347310.9:c.1781T=	ENSP00000321345.5:p.Phe594=
ENST00000395227.2:c.575T=	ENSP00000378652.2:p.Phe192=
ENST00000425614.3:c.1016T=	ENSP00000387640.2:p.Phe339=
ENST00000473881.2:c.*607T=	ENSP00000486667.1:n.*607T=
NM_144701.2:c.1781T=	NP_653302.2:p.Phe594=
XM_005270516.2:c.1019T=	XP_005270573.1:p.Phe340=
XM_011540789.1:c.1871T=	XP_011539091.1:p.Phe624=
XM_011540790.1:c.1781T=	XP_011539092.1:p.Phe594=
XM_011540791.1:c.1781T=	XP_011539093.1:p.Phe594=
XM_011540790.3:c.1781T=	XP_011539092.1:p.Phe594=
XM_011540791.3:c.1781T=	XP_011539093.1:p.Phe594=
XR_001736993.1:n.1861T=
NM_144701.3:c.1781T= MANE Select	NP_653302.2:p.Phe594=