Canonical Allele Identifier: CA340728669

Gene: IL23R

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1376G>T	ENSP00000513138.1:n.1376G>T
ENST00000697150.1:c.1434G>T	ENSP00000513139.1:n.1434G>T
ENST00000697151.1:c.1367G>T	ENSP00000513140.1:n.1367G>T
ENST00000697164.1:c.1447G>T	ENSP00000513153.1:p.Val483Phe
ENST00000697165.1:c.1234G>T	ENSP00000513154.1:p.Val412Phe
ENST00000347310.10:c.1537G>T MANE Select	ENSP00000321345.5:p.Val513Phe
ENST00000637002.1:c.928G>T	ENSP00000490340.1:p.Val310Phe
ENST00000347310.9:c.1537G>T	ENSP00000321345.5:p.Val513Phe
ENST00000395227.2:c.331G>T	ENSP00000378652.2:p.Val111Phe
ENST00000425614.3:c.772G>T	ENSP00000387640.2:p.Val258Phe
ENST00000473881.2:c.*363G>T	ENSP00000486667.1:n.*363G>T
NM_144701.2:c.1537G>T	NP_653302.2:p.Val513Phe
XM_005270516.2:c.775G>T	XP_005270573.1:p.Val259Phe
XM_011540789.1:c.1627G>T	XP_011539091.1:p.Val543Phe
XM_011540790.1:c.1537G>T	XP_011539092.1:p.Val513Phe
XM_011540791.1:c.1537G>T	XP_011539093.1:p.Val513Phe
XM_011540790.3:c.1537G>T	XP_011539092.1:p.Val513Phe
XM_011540791.3:c.1537G>T	XP_011539093.1:p.Val513Phe
XR_001736993.1:n.1617G>T
NM_144701.3:c.1537G>T MANE Select	NP_653302.2:p.Val513Phe