Canonical Allele Identifier: CA340730195

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259124A>C , CM000663.2:g.67259124A>C	GRCh38
NC_000001.10:g.67724807A>C , CM000663.1:g.67724807A>C	GRCh37
NC_000001.9:g.67497395A>C	NCBI36
NG_011498.1:g.97639A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_144701.3:c.1886A>C MANE Select	NP_653302.2:p.Lys629Thr
ENST00000347310.10:c.1886A>C MANE Select	ENSP00000321345.5:p.Lys629Thr
NM_144701.2:c.1886A>C	NP_653302.2:p.Lys629Thr
ENST00000347310.9:c.1886A>C	ENSP00000321345.5:p.Lys629Thr
ENST00000395227.2:c.680A>C	ENSP00000378652.2:p.Lys227Thr
ENST00000425614.3:c.1121A>C	ENSP00000387640.2:p.Lys374Thr
ENST00000473881.2:c.*712A>C	ENSP00000486667.1:n.*712A>C
ENST00000637002.1:c.1277A>C	ENSP00000490340.1:p.Lys426Thr
ENST00000697149.1:c.1725A>C	ENSP00000513138.1:n.1725A>C
ENST00000697150.1:c.1783A>C	ENSP00000513139.1:n.1783A>C
ENST00000697151.1:c.1716A>C	ENSP00000513140.1:n.1716A>C
ENST00000697164.1:c.1796A>C	ENSP00000513153.1:p.Lys599Thr
ENST00000697165.1:c.1583A>C	ENSP00000513154.1:p.Lys528Thr
XM_005270516.2:c.1124A>C	XP_005270573.1:p.Lys375Thr
XM_011540789.1:c.1976A>C	XP_011539091.1:p.Lys659Thr
XM_011540790.1:c.1886A>C	XP_011539092.1:p.Lys629Thr
XM_011540790.3:c.1886A>C	XP_011539092.1:p.Lys629Thr
XM_011540791.1:c.1886A>C	XP_011539093.1:p.Lys629Thr
XM_011540791.3:c.1886A>C	XP_011539093.1:p.Lys629Thr
XR_001736993.1:n.1966A>C