Canonical Allele Identifier: CA340729717

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259049A>G , CM000663.2:g.67259049A>G	GRCh38
NC_000001.10:g.67724732A>G , CM000663.1:g.67724732A>G	GRCh37
NC_000001.9:g.67497320A>G	NCBI36
NG_011498.1:g.97564A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_144701.3:c.1811A>G MANE Select	NP_653302.2:p.Glu604Gly
ENST00000347310.10:c.1811A>G MANE Select	ENSP00000321345.5:p.Glu604Gly
NM_144701.2:c.1811A>G	NP_653302.2:p.Glu604Gly
ENST00000347310.9:c.1811A>G	ENSP00000321345.5:p.Glu604Gly
ENST00000395227.2:c.605A>G	ENSP00000378652.2:p.Glu202Gly
ENST00000425614.3:c.1046A>G	ENSP00000387640.2:p.Glu349Gly
ENST00000473881.2:c.*637A>G	ENSP00000486667.1:n.*637A>G
ENST00000637002.1:c.1202A>G	ENSP00000490340.1:p.Glu401Gly
ENST00000697149.1:c.1650A>G	ENSP00000513138.1:n.1650A>G
ENST00000697150.1:c.1708A>G	ENSP00000513139.1:n.1708A>G
ENST00000697151.1:c.1641A>G	ENSP00000513140.1:n.1641A>G
ENST00000697164.1:c.1721A>G	ENSP00000513153.1:p.Glu574Gly
ENST00000697165.1:c.1508A>G	ENSP00000513154.1:p.Glu503Gly
XM_005270516.2:c.1049A>G	XP_005270573.1:p.Glu350Gly
XM_011540789.1:c.1901A>G	XP_011539091.1:p.Glu634Gly
XM_011540790.1:c.1811A>G	XP_011539092.1:p.Glu604Gly
XM_011540790.3:c.1811A>G	XP_011539092.1:p.Glu604Gly
XM_011540791.1:c.1811A>G	XP_011539093.1:p.Glu604Gly
XM_011540791.3:c.1811A>G	XP_011539093.1:p.Glu604Gly
XR_001736993.1:n.1891A>G