Canonical Allele Identifier: CA340729517

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724678A>T (hg19) ; chr1:g.67258995A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258995A>T , CM000663.2:g.67258995A>T	GRCh38
NC_000001.10:g.67724678A>T , CM000663.1:g.67724678A>T	GRCh37
NC_000001.9:g.67497266A>T	NCBI36
NG_011498.1:g.97510A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1596A>T	ENSP00000513138.1:n.1596A>T
ENST00000697150.1:c.1654A>T	ENSP00000513139.1:n.1654A>T
ENST00000697151.1:c.1587A>T	ENSP00000513140.1:n.1587A>T
ENST00000697164.1:c.1667A>T	ENSP00000513153.1:p.Glu556Val
ENST00000697165.1:c.1454A>T	ENSP00000513154.1:p.Glu485Val
ENST00000347310.10:c.1757A>T MANE Select	ENSP00000321345.5:p.Glu586Val
ENST00000637002.1:c.1148A>T	ENSP00000490340.1:p.Glu383Val
ENST00000347310.9:c.1757A>T	ENSP00000321345.5:p.Glu586Val
ENST00000395227.2:c.551A>T	ENSP00000378652.2:p.Glu184Val
ENST00000425614.3:c.992A>T	ENSP00000387640.2:p.Glu331Val
ENST00000473881.2:c.*583A>T	ENSP00000486667.1:n.*583A>T
NM_144701.2:c.1757A>T	NP_653302.2:p.Glu586Val
XM_005270516.2:c.995A>T	XP_005270573.1:p.Glu332Val
XM_011540789.1:c.1847A>T	XP_011539091.1:p.Glu616Val
XM_011540790.1:c.1757A>T	XP_011539092.1:p.Glu586Val
XM_011540791.1:c.1757A>T	XP_011539093.1:p.Glu586Val
XM_011540790.3:c.1757A>T	XP_011539092.1:p.Glu586Val
XM_011540791.3:c.1757A>T	XP_011539093.1:p.Glu586Val
XR_001736993.1:n.1837A>T
NM_144701.3:c.1757A>T MANE Select	NP_653302.2:p.Glu586Val