Canonical Allele Identifier: CA340729325

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724627A>T (hg19) ; chr1:g.67258944A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258944A>T , CM000663.2:g.67258944A>T	GRCh38
NC_000001.10:g.67724627A>T , CM000663.1:g.67724627A>T	GRCh37
NC_000001.9:g.67497215A>T	NCBI36
NG_011498.1:g.97459A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1545A>T	ENSP00000513138.1:n.1545A>T
ENST00000697150.1:c.1603A>T	ENSP00000513139.1:n.1603A>T
ENST00000697151.1:c.1536A>T	ENSP00000513140.1:n.1536A>T
ENST00000697164.1:c.1616A>T	ENSP00000513153.1:p.Glu539Val
ENST00000697165.1:c.1403A>T	ENSP00000513154.1:p.Glu468Val
ENST00000347310.10:c.1706A>T MANE Select	ENSP00000321345.5:p.Glu569Val
ENST00000637002.1:c.1097A>T	ENSP00000490340.1:p.Glu366Val
ENST00000347310.9:c.1706A>T	ENSP00000321345.5:p.Glu569Val
ENST00000395227.2:c.500A>T	ENSP00000378652.2:p.Glu167Val
ENST00000425614.3:c.941A>T	ENSP00000387640.2:p.Glu314Val
ENST00000473881.2:c.*532A>T	ENSP00000486667.1:n.*532A>T
NM_144701.2:c.1706A>T	NP_653302.2:p.Glu569Val
XM_005270516.2:c.944A>T	XP_005270573.1:p.Glu315Val
XM_011540789.1:c.1796A>T	XP_011539091.1:p.Glu599Val
XM_011540790.1:c.1706A>T	XP_011539092.1:p.Glu569Val
XM_011540791.1:c.1706A>T	XP_011539093.1:p.Glu569Val
XM_011540790.3:c.1706A>T	XP_011539092.1:p.Glu569Val
XM_011540791.3:c.1706A>T	XP_011539093.1:p.Glu569Val
XR_001736993.1:n.1786A>T
NM_144701.3:c.1706A>T MANE Select	NP_653302.2:p.Glu569Val