Canonical Allele Identifier: CA1173064250

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258748A= , CM000663.2:g.67258748A=	GRCh38
NC_000001.10:g.67724431A= , CM000663.1:g.67724431A=	GRCh37
NC_000001.9:g.67497019A=	NCBI36
NG_011498.1:g.97263A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1349A=	ENSP00000513138.1:n.1349A=
ENST00000697150.1:c.1407A=	ENSP00000513139.1:n.1407A=
ENST00000697151.1:c.1340A=	ENSP00000513140.1:n.1340A=
ENST00000697164.1:c.1420A=	ENSP00000513153.1:p.Ile474=
ENST00000697165.1:c.1207A=	ENSP00000513154.1:p.Ile403=
ENST00000347310.10:c.1510A= MANE Select	ENSP00000321345.5:p.Ile504=
ENST00000637002.1:c.901A=	ENSP00000490340.1:p.Ile301=
ENST00000347310.9:c.1510A=	ENSP00000321345.5:p.Ile504=
ENST00000395227.2:c.304A=	ENSP00000378652.2:p.Ile102=
ENST00000425614.3:c.745A=	ENSP00000387640.2:p.Ile249=
ENST00000473881.2:c.*336A=	ENSP00000486667.1:n.*336A=
NM_144701.2:c.1510A=	NP_653302.2:p.Ile504=
XM_005270516.2:c.748A=	XP_005270573.1:p.Ile250=
XM_011540789.1:c.1600A=	XP_011539091.1:p.Ile534=
XM_011540790.1:c.1510A=	XP_011539092.1:p.Ile504=
XM_011540791.1:c.1510A=	XP_011539093.1:p.Ile504=
XM_011540790.3:c.1510A=	XP_011539092.1:p.Ile504=
XM_011540791.3:c.1510A=	XP_011539093.1:p.Ile504=
XR_001736993.1:n.1590A=
NM_144701.3:c.1510A= MANE Select	NP_653302.2:p.Ile504=