Canonical Allele Identifier: CA340728667

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724458G>A (hg19) ; chr1:g.67258775G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258775G>A , CM000663.2:g.67258775G>A	GRCh38
NC_000001.10:g.67724458G>A , CM000663.1:g.67724458G>A	GRCh37
NC_000001.9:g.67497046G>A	NCBI36
NG_011498.1:g.97290G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1376G>A	ENSP00000513138.1:n.1376G>A
ENST00000697150.1:c.1434G>A	ENSP00000513139.1:n.1434G>A
ENST00000697151.1:c.1367G>A	ENSP00000513140.1:n.1367G>A
ENST00000697164.1:c.1447G>A	ENSP00000513153.1:p.Val483Ile
ENST00000697165.1:c.1234G>A	ENSP00000513154.1:p.Val412Ile
ENST00000347310.10:c.1537G>A MANE Select	ENSP00000321345.5:p.Val513Ile
ENST00000637002.1:c.928G>A	ENSP00000490340.1:p.Val310Ile
ENST00000347310.9:c.1537G>A	ENSP00000321345.5:p.Val513Ile
ENST00000395227.2:c.331G>A	ENSP00000378652.2:p.Val111Ile
ENST00000425614.3:c.772G>A	ENSP00000387640.2:p.Val258Ile
ENST00000473881.2:c.*363G>A	ENSP00000486667.1:n.*363G>A
NM_144701.2:c.1537G>A	NP_653302.2:p.Val513Ile
XM_005270516.2:c.775G>A	XP_005270573.1:p.Val259Ile
XM_011540789.1:c.1627G>A	XP_011539091.1:p.Val543Ile
XM_011540790.1:c.1537G>A	XP_011539092.1:p.Val513Ile
XM_011540791.1:c.1537G>A	XP_011539093.1:p.Val513Ile
XM_011540790.3:c.1537G>A	XP_011539092.1:p.Val513Ile
XM_011540791.3:c.1537G>A	XP_011539093.1:p.Val513Ile
XR_001736993.1:n.1617G>A
NM_144701.3:c.1537G>A MANE Select	NP_653302.2:p.Val513Ile