Canonical Allele Identifier: CA340730069

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259108A>G , CM000663.2:g.67259108A>G	GRCh38
NC_000001.10:g.67724791A>G , CM000663.1:g.67724791A>G	GRCh37
NC_000001.9:g.67497379A>G	NCBI36
NG_011498.1:g.97623A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_144701.3:c.1870A>G MANE Select	NP_653302.2:p.Ile624Val
ENST00000347310.10:c.1870A>G MANE Select	ENSP00000321345.5:p.Ile624Val
NM_144701.2:c.1870A>G	NP_653302.2:p.Ile624Val
ENST00000347310.9:c.1870A>G	ENSP00000321345.5:p.Ile624Val
ENST00000395227.2:c.664A>G	ENSP00000378652.2:p.Ile222Val
ENST00000425614.3:c.1105A>G	ENSP00000387640.2:p.Ile369Val
ENST00000473881.2:c.*696A>G	ENSP00000486667.1:n.*696A>G
ENST00000637002.1:c.1261A>G	ENSP00000490340.1:p.Ile421Val
ENST00000697149.1:c.1709A>G	ENSP00000513138.1:n.1709A>G
ENST00000697150.1:c.1767A>G	ENSP00000513139.1:n.1767A>G
ENST00000697151.1:c.1700A>G	ENSP00000513140.1:n.1700A>G
ENST00000697164.1:c.1780A>G	ENSP00000513153.1:p.Ile594Val
ENST00000697165.1:c.1567A>G	ENSP00000513154.1:p.Ile523Val
XM_005270516.2:c.1108A>G	XP_005270573.1:p.Ile370Val
XM_011540789.1:c.1960A>G	XP_011539091.1:p.Ile654Val
XM_011540790.1:c.1870A>G	XP_011539092.1:p.Ile624Val
XM_011540790.3:c.1870A>G	XP_011539092.1:p.Ile624Val
XM_011540791.1:c.1870A>G	XP_011539093.1:p.Ile624Val
XM_011540791.3:c.1870A>G	XP_011539093.1:p.Ile624Val
XR_001736993.1:n.1950A>G