Canonical Allele Identifier: CA3081745124

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259075C= , CM000663.2:g.67259075C=	GRCh38
NC_000001.10:g.67724758C= , CM000663.1:g.67724758C=	GRCh37
NC_000001.9:g.67497346C=	NCBI36
NG_011498.1:g.97590C=

Transcript Alleles

HGVS	Amino-acid Change
NM_144701.3:c.1837C= MANE Select	NP_653302.2:p.Pro613=
ENST00000347310.10:c.1837C= MANE Select	ENSP00000321345.5:p.Pro613=
NM_144701.2:c.1837C=	NP_653302.2:p.Pro613=
ENST00000347310.9:c.1837C=	ENSP00000321345.5:p.Pro613=
ENST00000395227.2:c.631C=	ENSP00000378652.2:p.Pro211=
ENST00000425614.3:c.1072C=	ENSP00000387640.2:p.Pro358=
ENST00000473881.2:c.*663C=	ENSP00000486667.1:n.*663C=
ENST00000637002.1:c.1228C=	ENSP00000490340.1:p.Pro410=
ENST00000697149.1:c.1676C=	ENSP00000513138.1:n.1676C=
ENST00000697150.1:c.1734C=	ENSP00000513139.1:n.1734C=
ENST00000697151.1:c.1667C=	ENSP00000513140.1:n.1667C=
ENST00000697164.1:c.1747C=	ENSP00000513153.1:p.Pro583=
ENST00000697165.1:c.1534C=	ENSP00000513154.1:p.Pro512=
XM_005270516.2:c.1075C=	XP_005270573.1:p.Pro359=
XM_011540789.1:c.1927C=	XP_011539091.1:p.Pro643=
XM_011540790.1:c.1837C=	XP_011539092.1:p.Pro613=
XM_011540790.3:c.1837C=	XP_011539092.1:p.Pro613=
XM_011540791.1:c.1837C=	XP_011539093.1:p.Pro613=
XM_011540791.3:c.1837C=	XP_011539093.1:p.Pro613=
XR_001736993.1:n.1917C=