Canonical Allele Identifier: CA3081745108

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259067C= , CM000663.2:g.67259067C=	GRCh38
NC_000001.10:g.67724750C= , CM000663.1:g.67724750C=	GRCh37
NC_000001.9:g.67497338C=	NCBI36
NG_011498.1:g.97582C=

Transcript Alleles

HGVS	Amino-acid Change
NM_144701.3:c.1829C= MANE Select	NP_653302.2:p.Thr610=
ENST00000347310.10:c.1829C= MANE Select	ENSP00000321345.5:p.Thr610=
NM_144701.2:c.1829C=	NP_653302.2:p.Thr610=
ENST00000347310.9:c.1829C=	ENSP00000321345.5:p.Thr610=
ENST00000395227.2:c.623C=	ENSP00000378652.2:p.Thr208=
ENST00000425614.3:c.1064C=	ENSP00000387640.2:p.Thr355=
ENST00000473881.2:c.*655C=	ENSP00000486667.1:n.*655C=
ENST00000637002.1:c.1220C=	ENSP00000490340.1:p.Thr407=
ENST00000697149.1:c.1668C=	ENSP00000513138.1:n.1668C=
ENST00000697150.1:c.1726C=	ENSP00000513139.1:n.1726C=
ENST00000697151.1:c.1659C=	ENSP00000513140.1:n.1659C=
ENST00000697164.1:c.1739C=	ENSP00000513153.1:p.Thr580=
ENST00000697165.1:c.1526C=	ENSP00000513154.1:p.Thr509=
XM_005270516.2:c.1067C=	XP_005270573.1:p.Thr356=
XM_011540789.1:c.1919C=	XP_011539091.1:p.Thr640=
XM_011540790.1:c.1829C=	XP_011539092.1:p.Thr610=
XM_011540790.3:c.1829C=	XP_011539092.1:p.Thr610=
XM_011540791.1:c.1829C=	XP_011539093.1:p.Thr610=
XM_011540791.3:c.1829C=	XP_011539093.1:p.Thr610=
XR_001736993.1:n.1909C=