Canonical Allele Identifier: CA340728673

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724461G>T (hg19) ; chr1:g.67258778G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258778G>T , CM000663.2:g.67258778G>T	GRCh38
NC_000001.10:g.67724461G>T , CM000663.1:g.67724461G>T	GRCh37
NC_000001.9:g.67497049G>T	NCBI36
NG_011498.1:g.97293G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1379G>T	ENSP00000513138.1:n.1379G>T
ENST00000697150.1:c.1437G>T	ENSP00000513139.1:n.1437G>T
ENST00000697151.1:c.1370G>T	ENSP00000513140.1:n.1370G>T
ENST00000697164.1:c.1450G>T	ENSP00000513153.1:p.Asp484Tyr
ENST00000697165.1:c.1237G>T	ENSP00000513154.1:p.Asp413Tyr
ENST00000347310.10:c.1540G>T MANE Select	ENSP00000321345.5:p.Asp514Tyr
ENST00000637002.1:c.931G>T	ENSP00000490340.1:p.Asp311Tyr
ENST00000347310.9:c.1540G>T	ENSP00000321345.5:p.Asp514Tyr
ENST00000395227.2:c.334G>T	ENSP00000378652.2:p.Asp112Tyr
ENST00000425614.3:c.775G>T	ENSP00000387640.2:p.Asp259Tyr
ENST00000473881.2:c.*366G>T	ENSP00000486667.1:n.*366G>T
NM_144701.2:c.1540G>T	NP_653302.2:p.Asp514Tyr
XM_005270516.2:c.778G>T	XP_005270573.1:p.Asp260Tyr
XM_011540789.1:c.1630G>T	XP_011539091.1:p.Asp544Tyr
XM_011540790.1:c.1540G>T	XP_011539092.1:p.Asp514Tyr
XM_011540791.1:c.1540G>T	XP_011539093.1:p.Asp514Tyr
XM_011540790.3:c.1540G>T	XP_011539092.1:p.Asp514Tyr
XM_011540791.3:c.1540G>T	XP_011539093.1:p.Asp514Tyr
XR_001736993.1:n.1620G>T
NM_144701.3:c.1540G>T MANE Select	NP_653302.2:p.Asp514Tyr