Canonical Allele Identifier: CA1173064286

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258887G= , CM000663.2:g.67258887G=	GRCh38
NC_000001.10:g.67724570G= , CM000663.1:g.67724570G=	GRCh37
NC_000001.9:g.67497158G=	NCBI36
NG_011498.1:g.97402G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1488G=	ENSP00000513138.1:n.1488G=
ENST00000697150.1:c.1546G=	ENSP00000513139.1:n.1546G=
ENST00000697151.1:c.1479G=	ENSP00000513140.1:n.1479G=
ENST00000697164.1:c.1559G=	ENSP00000513153.1:p.Ser520=
ENST00000697165.1:c.1346G=	ENSP00000513154.1:p.Ser449=
ENST00000347310.10:c.1649G= MANE Select	ENSP00000321345.5:p.Ser550=
ENST00000637002.1:c.1040G=	ENSP00000490340.1:p.Ser347=
ENST00000347310.9:c.1649G=	ENSP00000321345.5:p.Ser550=
ENST00000395227.2:c.443G=	ENSP00000378652.2:p.Ser148=
ENST00000425614.3:c.884G=	ENSP00000387640.2:p.Ser295=
ENST00000473881.2:c.*475G=	ENSP00000486667.1:n.*475G=
NM_144701.2:c.1649G=	NP_653302.2:p.Ser550=
XM_005270516.2:c.887G=	XP_005270573.1:p.Ser296=
XM_011540789.1:c.1739G=	XP_011539091.1:p.Ser580=
XM_011540790.1:c.1649G=	XP_011539092.1:p.Ser550=
XM_011540791.1:c.1649G=	XP_011539093.1:p.Ser550=
XM_011540790.3:c.1649G=	XP_011539092.1:p.Ser550=
XM_011540791.3:c.1649G=	XP_011539093.1:p.Ser550=
XR_001736993.1:n.1729G=
NM_144701.3:c.1649G= MANE Select	NP_653302.2:p.Ser550=