Canonical Allele Identifier: CA340729414

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724648A>T (hg19) ; chr1:g.67258965A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258965A>T , CM000663.2:g.67258965A>T	GRCh38
NC_000001.10:g.67724648A>T , CM000663.1:g.67724648A>T	GRCh37
NC_000001.9:g.67497236A>T	NCBI36
NG_011498.1:g.97480A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1566A>T	ENSP00000513138.1:n.1566A>T
ENST00000697150.1:c.1624A>T	ENSP00000513139.1:n.1624A>T
ENST00000697151.1:c.1557A>T	ENSP00000513140.1:n.1557A>T
ENST00000697164.1:c.1637A>T	ENSP00000513153.1:p.Glu546Val
ENST00000697165.1:c.1424A>T	ENSP00000513154.1:p.Glu475Val
ENST00000347310.10:c.1727A>T MANE Select	ENSP00000321345.5:p.Glu576Val
ENST00000637002.1:c.1118A>T	ENSP00000490340.1:p.Glu373Val
ENST00000347310.9:c.1727A>T	ENSP00000321345.5:p.Glu576Val
ENST00000395227.2:c.521A>T	ENSP00000378652.2:p.Glu174Val
ENST00000425614.3:c.962A>T	ENSP00000387640.2:p.Glu321Val
ENST00000473881.2:c.*553A>T	ENSP00000486667.1:n.*553A>T
NM_144701.2:c.1727A>T	NP_653302.2:p.Glu576Val
XM_005270516.2:c.965A>T	XP_005270573.1:p.Glu322Val
XM_011540789.1:c.1817A>T	XP_011539091.1:p.Glu606Val
XM_011540790.1:c.1727A>T	XP_011539092.1:p.Glu576Val
XM_011540791.1:c.1727A>T	XP_011539093.1:p.Glu576Val
XM_011540790.3:c.1727A>T	XP_011539092.1:p.Glu576Val
XM_011540791.3:c.1727A>T	XP_011539093.1:p.Glu576Val
XR_001736993.1:n.1807A>T
NM_144701.3:c.1727A>T MANE Select	NP_653302.2:p.Glu576Val