Canonical Allele Identifier: CA340729966

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259096C>T , CM000663.2:g.67259096C>T	GRCh38
NC_000001.10:g.67724779C>T , CM000663.1:g.67724779C>T	GRCh37
NC_000001.9:g.67497367C>T	NCBI36
NG_011498.1:g.97611C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_144701.3:c.1858C>T MANE Select	NP_653302.2:p.His620Tyr
ENST00000347310.10:c.1858C>T MANE Select	ENSP00000321345.5:p.His620Tyr
NM_144701.2:c.1858C>T	NP_653302.2:p.His620Tyr
ENST00000347310.9:c.1858C>T	ENSP00000321345.5:p.His620Tyr
ENST00000395227.2:c.652C>T	ENSP00000378652.2:p.His218Tyr
ENST00000425614.3:c.1093C>T	ENSP00000387640.2:p.His365Tyr
ENST00000473881.2:c.*684C>T	ENSP00000486667.1:n.*684C>T
ENST00000637002.1:c.1249C>T	ENSP00000490340.1:p.His417Tyr
ENST00000697149.1:c.1697C>T	ENSP00000513138.1:n.1697C>T
ENST00000697150.1:c.1755C>T	ENSP00000513139.1:n.1755C>T
ENST00000697151.1:c.1688C>T	ENSP00000513140.1:n.1688C>T
ENST00000697164.1:c.1768C>T	ENSP00000513153.1:p.His590Tyr
ENST00000697165.1:c.1555C>T	ENSP00000513154.1:p.His519Tyr
XM_005270516.2:c.1096C>T	XP_005270573.1:p.His366Tyr
XM_011540789.1:c.1948C>T	XP_011539091.1:p.His650Tyr
XM_011540790.1:c.1858C>T	XP_011539092.1:p.His620Tyr
XM_011540790.3:c.1858C>T	XP_011539092.1:p.His620Tyr
XM_011540791.1:c.1858C>T	XP_011539093.1:p.His620Tyr
XM_011540791.3:c.1858C>T	XP_011539093.1:p.His620Tyr
XR_001736993.1:n.1938C>T