Canonical Allele Identifier: CA340729939

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724774A>T (hg19) ; chr1:g.67259091A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259091A>T , CM000663.2:g.67259091A>T	GRCh38
NC_000001.10:g.67724774A>T , CM000663.1:g.67724774A>T	GRCh37
NC_000001.9:g.67497362A>T	NCBI36
NG_011498.1:g.97606A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1692A>T	ENSP00000513138.1:n.1692A>T
ENST00000697150.1:c.1750A>T	ENSP00000513139.1:n.1750A>T
ENST00000697151.1:c.1683A>T	ENSP00000513140.1:n.1683A>T
ENST00000697164.1:c.1763A>T	ENSP00000513153.1:p.Glu588Val
ENST00000697165.1:c.1550A>T	ENSP00000513154.1:p.Glu517Val
ENST00000347310.10:c.1853A>T MANE Select	ENSP00000321345.5:p.Glu618Val
ENST00000637002.1:c.1244A>T	ENSP00000490340.1:p.Glu415Val
ENST00000347310.9:c.1853A>T	ENSP00000321345.5:p.Glu618Val
ENST00000395227.2:c.647A>T	ENSP00000378652.2:p.Glu216Val
ENST00000425614.3:c.1088A>T	ENSP00000387640.2:p.Glu363Val
ENST00000473881.2:c.*679A>T	ENSP00000486667.1:n.*679A>T
NM_144701.2:c.1853A>T	NP_653302.2:p.Glu618Val
XM_005270516.2:c.1091A>T	XP_005270573.1:p.Glu364Val
XM_011540789.1:c.1943A>T	XP_011539091.1:p.Glu648Val
XM_011540790.1:c.1853A>T	XP_011539092.1:p.Glu618Val
XM_011540791.1:c.1853A>T	XP_011539093.1:p.Glu618Val
XM_011540790.3:c.1853A>T	XP_011539092.1:p.Glu618Val
XM_011540791.3:c.1853A>T	XP_011539093.1:p.Glu618Val
XR_001736993.1:n.1933A>T
NM_144701.3:c.1853A>T MANE Select	NP_653302.2:p.Glu618Val