Canonical Allele Identifier: CA1173064450

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259356G= , CM000663.2:g.67259356G=	GRCh38
NC_000001.10:g.67725039G= , CM000663.1:g.67725039G=	GRCh37
NC_000001.9:g.67497627G=	NCBI36
NG_011498.1:g.97871G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000347310.10:c.*228G= MANE Select	ENSP00000321345.5:n.*228G=
ENST00000347310.9:c.*228G=	ENSP00000321345.5:n.*228G=
ENST00000395227.2:c.*228G=	ENSP00000378652.2:n.*228G=
ENST00000473881.2:c.*944G=	ENSP00000486667.1:n.*944G=
NM_144701.2:c.*228G=	NP_653302.2:n.*228G=
XM_005270516.2:c.*228G=	XP_005270573.1:n.*228G=
XM_011540789.1:c.*228G=	XP_011539091.1:n.*228G=
XM_011540790.1:c.*228G=	XP_011539092.1:n.*228G=
XM_011540791.1:c.*228G=	XP_011539093.1:n.*228G=
XM_011540790.3:c.*228G=	XP_011539092.1:n.*228G=
XM_011540791.3:c.*228G=	XP_011539093.1:n.*228G=
NM_144701.3:c.*228G= MANE Select	NP_653302.2:n.*228G=