Canonical Allele Identifier: CA340730167

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259120G>C , CM000663.2:g.67259120G>C	GRCh38
NC_000001.10:g.67724803G>C , CM000663.1:g.67724803G>C	GRCh37
NC_000001.9:g.67497391G>C	NCBI36
NG_011498.1:g.97635G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_144701.3:c.1882G>C MANE Select	NP_653302.2:p.Glu628Gln
ENST00000347310.10:c.1882G>C MANE Select	ENSP00000321345.5:p.Glu628Gln
NM_144701.2:c.1882G>C	NP_653302.2:p.Glu628Gln
ENST00000347310.9:c.1882G>C	ENSP00000321345.5:p.Glu628Gln
ENST00000395227.2:c.676G>C	ENSP00000378652.2:p.Glu226Gln
ENST00000425614.3:c.1117G>C	ENSP00000387640.2:p.Glu373Gln
ENST00000473881.2:c.*708G>C	ENSP00000486667.1:n.*708G>C
ENST00000637002.1:c.1273G>C	ENSP00000490340.1:p.Glu425Gln
ENST00000697149.1:c.1721G>C	ENSP00000513138.1:n.1721G>C
ENST00000697150.1:c.1779G>C	ENSP00000513139.1:n.1779G>C
ENST00000697151.1:c.1712G>C	ENSP00000513140.1:n.1712G>C
ENST00000697164.1:c.1792G>C	ENSP00000513153.1:p.Glu598Gln
ENST00000697165.1:c.1579G>C	ENSP00000513154.1:p.Glu527Gln
XM_005270516.2:c.1120G>C	XP_005270573.1:p.Glu374Gln
XM_011540789.1:c.1972G>C	XP_011539091.1:p.Glu658Gln
XM_011540790.1:c.1882G>C	XP_011539092.1:p.Glu628Gln
XM_011540790.3:c.1882G>C	XP_011539092.1:p.Glu628Gln
XM_011540791.1:c.1882G>C	XP_011539093.1:p.Glu628Gln
XM_011540791.3:c.1882G>C	XP_011539093.1:p.Glu628Gln
XR_001736993.1:n.1962G>C