Canonical Allele Identifier: CA900068

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259126T>C , CM000663.2:g.67259126T>C	GRCh38
NC_000001.10:g.67724809T>C , CM000663.1:g.67724809T>C	GRCh37
NC_000001.9:g.67497397T>C	NCBI36
NG_011498.1:g.97641T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_144701.3:c.1888T>C MANE Select	NP_653302.2:p.Ter630Gln
ENST00000347310.10:c.1888T>C MANE Select	ENSP00000321345.5:p.Ter630Gln
NM_144701.2:c.1888T>C	NP_653302.2:p.Ter630Gln
ENST00000347310.9:c.1888T>C	ENSP00000321345.5:p.Ter630Gln
ENST00000395227.2:c.682T>C	ENSP00000378652.2:p.Ter228Gln
ENST00000425614.3:c.1123T>C	ENSP00000387640.2:p.Ter375Gln
ENST00000473881.2:c.*714T>C	ENSP00000486667.1:n.*714T>C
ENST00000637002.1:c.1279T>C	ENSP00000490340.1:p.Ter427Gln
ENST00000697164.1:c.1798T>C	ENSP00000513153.1:p.Ter600Gln
ENST00000697165.1:c.1585T>C	ENSP00000513154.1:p.Ter529Gln
XM_005270516.2:c.1126T>C	XP_005270573.1:p.Ter376Gln
XM_011540789.1:c.1978T>C	XP_011539091.1:p.Ter660Gln
XM_011540790.1:c.1888T>C	XP_011539092.1:p.Ter630Gln
XM_011540790.3:c.1888T>C	XP_011539092.1:p.Ter630Gln
XM_011540791.1:c.1888T>C	XP_011539093.1:p.Ter630Gln
XM_011540791.3:c.1888T>C	XP_011539093.1:p.Ter630Gln