Canonical Allele Identifier: CA418438757

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259035G>C , CM000663.2:g.67259035G>C	GRCh38
NC_000001.10:g.67724718G>C , CM000663.1:g.67724718G>C	GRCh37
NC_000001.9:g.67497306G>C	NCBI36
NG_011498.1:g.97550G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_144701.3:c.1797G>C MANE Select	NP_653302.2:p.Gly599=
ENST00000347310.10:c.1797G>C MANE Select	ENSP00000321345.5:p.Gly599=
NM_144701.2:c.1797G>C	NP_653302.2:p.Gly599=
ENST00000347310.9:c.1797G>C	ENSP00000321345.5:p.Gly599=
ENST00000395227.2:c.591G>C	ENSP00000378652.2:p.Gly197=
ENST00000425614.3:c.1032G>C	ENSP00000387640.2:p.Gly344=
ENST00000473881.2:c.*623G>C	ENSP00000486667.1:n.*623G>C
ENST00000637002.1:c.1188G>C	ENSP00000490340.1:p.Gly396=
ENST00000697149.1:c.1636G>C	ENSP00000513138.1:n.1636G>C
ENST00000697150.1:c.1694G>C	ENSP00000513139.1:n.1694G>C
ENST00000697151.1:c.1627G>C	ENSP00000513140.1:n.1627G>C
ENST00000697164.1:c.1707G>C	ENSP00000513153.1:p.Gly569=
ENST00000697165.1:c.1494G>C	ENSP00000513154.1:p.Gly498=
XM_005270516.2:c.1035G>C	XP_005270573.1:p.Gly345=
XM_011540789.1:c.1887G>C	XP_011539091.1:p.Gly629=
XM_011540790.1:c.1797G>C	XP_011539092.1:p.Gly599=
XM_011540790.3:c.1797G>C	XP_011539092.1:p.Gly599=
XM_011540791.1:c.1797G>C	XP_011539093.1:p.Gly599=
XM_011540791.3:c.1797G>C	XP_011539093.1:p.Gly599=
XR_001736993.1:n.1877G>C