Canonical Allele Identifier: CA340729632

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259027T>C , CM000663.2:g.67259027T>C	GRCh38
NC_000001.10:g.67724710T>C , CM000663.1:g.67724710T>C	GRCh37
NC_000001.9:g.67497298T>C	NCBI36
NG_011498.1:g.97542T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_144701.3:c.1789T>C MANE Select	NP_653302.2:p.Cys597Arg
ENST00000347310.10:c.1789T>C MANE Select	ENSP00000321345.5:p.Cys597Arg
NM_144701.2:c.1789T>C	NP_653302.2:p.Cys597Arg
ENST00000347310.9:c.1789T>C	ENSP00000321345.5:p.Cys597Arg
ENST00000395227.2:c.583T>C	ENSP00000378652.2:p.Cys195Arg
ENST00000425614.3:c.1024T>C	ENSP00000387640.2:p.Cys342Arg
ENST00000473881.2:c.*615T>C	ENSP00000486667.1:n.*615T>C
ENST00000637002.1:c.1180T>C	ENSP00000490340.1:p.Cys394Arg
ENST00000697149.1:c.1628T>C	ENSP00000513138.1:n.1628T>C
ENST00000697150.1:c.1686T>C	ENSP00000513139.1:n.1686T>C
ENST00000697151.1:c.1619T>C	ENSP00000513140.1:n.1619T>C
ENST00000697164.1:c.1699T>C	ENSP00000513153.1:p.Cys567Arg
ENST00000697165.1:c.1486T>C	ENSP00000513154.1:p.Cys496Arg
XM_005270516.2:c.1027T>C	XP_005270573.1:p.Cys343Arg
XM_011540789.1:c.1879T>C	XP_011539091.1:p.Cys627Arg
XM_011540790.1:c.1789T>C	XP_011539092.1:p.Cys597Arg
XM_011540790.3:c.1789T>C	XP_011539092.1:p.Cys597Arg
XM_011540791.1:c.1789T>C	XP_011539093.1:p.Cys597Arg
XM_011540791.3:c.1789T>C	XP_011539093.1:p.Cys597Arg
XR_001736993.1:n.1869T>C