Canonical Allele Identifier: CA340730093

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259111T>A , CM000663.2:g.67259111T>A	GRCh38
NC_000001.10:g.67724794T>A , CM000663.1:g.67724794T>A	GRCh37
NC_000001.9:g.67497382T>A	NCBI36
NG_011498.1:g.97626T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_144701.3:c.1873T>A MANE Select	NP_653302.2:p.Ser625Thr
ENST00000347310.10:c.1873T>A MANE Select	ENSP00000321345.5:p.Ser625Thr
NM_144701.2:c.1873T>A	NP_653302.2:p.Ser625Thr
ENST00000347310.9:c.1873T>A	ENSP00000321345.5:p.Ser625Thr
ENST00000395227.2:c.667T>A	ENSP00000378652.2:p.Ser223Thr
ENST00000425614.3:c.1108T>A	ENSP00000387640.2:p.Ser370Thr
ENST00000473881.2:c.*699T>A	ENSP00000486667.1:n.*699T>A
ENST00000637002.1:c.1264T>A	ENSP00000490340.1:p.Ser422Thr
ENST00000697149.1:c.1712T>A	ENSP00000513138.1:n.1712T>A
ENST00000697150.1:c.1770T>A	ENSP00000513139.1:n.1770T>A
ENST00000697151.1:c.1703T>A	ENSP00000513140.1:n.1703T>A
ENST00000697164.1:c.1783T>A	ENSP00000513153.1:p.Ser595Thr
ENST00000697165.1:c.1570T>A	ENSP00000513154.1:p.Ser524Thr
XM_005270516.2:c.1111T>A	XP_005270573.1:p.Ser371Thr
XM_011540789.1:c.1963T>A	XP_011539091.1:p.Ser655Thr
XM_011540790.1:c.1873T>A	XP_011539092.1:p.Ser625Thr
XM_011540790.3:c.1873T>A	XP_011539092.1:p.Ser625Thr
XM_011540791.1:c.1873T>A	XP_011539093.1:p.Ser625Thr
XM_011540791.3:c.1873T>A	XP_011539093.1:p.Ser625Thr
XR_001736993.1:n.1953T>A