Canonical Allele Identifier: CA3081745031

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259031T= , CM000663.2:g.67259031T=	GRCh38
NC_000001.10:g.67724714T= , CM000663.1:g.67724714T=	GRCh37
NC_000001.9:g.67497302T=	NCBI36
NG_011498.1:g.97546T=

Transcript Alleles

HGVS	Amino-acid Change
NM_144701.3:c.1793T= MANE Select	NP_653302.2:p.Leu598=
ENST00000347310.10:c.1793T= MANE Select	ENSP00000321345.5:p.Leu598=
NM_144701.2:c.1793T=	NP_653302.2:p.Leu598=
ENST00000347310.9:c.1793T=	ENSP00000321345.5:p.Leu598=
ENST00000395227.2:c.587T=	ENSP00000378652.2:p.Leu196=
ENST00000425614.3:c.1028T=	ENSP00000387640.2:p.Leu343=
ENST00000473881.2:c.*619T=	ENSP00000486667.1:n.*619T=
ENST00000637002.1:c.1184T=	ENSP00000490340.1:p.Leu395=
ENST00000697149.1:c.1632T=	ENSP00000513138.1:n.1632T=
ENST00000697150.1:c.1690T=	ENSP00000513139.1:n.1690T=
ENST00000697151.1:c.1623T=	ENSP00000513140.1:n.1623T=
ENST00000697164.1:c.1703T=	ENSP00000513153.1:p.Leu568=
ENST00000697165.1:c.1490T=	ENSP00000513154.1:p.Leu497=
XM_005270516.2:c.1031T=	XP_005270573.1:p.Leu344=
XM_011540789.1:c.1883T=	XP_011539091.1:p.Leu628=
XM_011540790.1:c.1793T=	XP_011539092.1:p.Leu598=
XM_011540790.3:c.1793T=	XP_011539092.1:p.Leu598=
XM_011540791.1:c.1793T=	XP_011539093.1:p.Leu598=
XM_011540791.3:c.1793T=	XP_011539093.1:p.Leu598=
XR_001736993.1:n.1873T=