Canonical Allele Identifier: CA340729173

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724592A>T (hg19) ; chr1:g.67258909A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258909A>T , CM000663.2:g.67258909A>T	GRCh38
NC_000001.10:g.67724592A>T , CM000663.1:g.67724592A>T	GRCh37
NC_000001.9:g.67497180A>T	NCBI36
NG_011498.1:g.97424A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1510A>T	ENSP00000513138.1:n.1510A>T
ENST00000697150.1:c.1568A>T	ENSP00000513139.1:n.1568A>T
ENST00000697151.1:c.1501A>T	ENSP00000513140.1:n.1501A>T
ENST00000697164.1:c.1581A>T	ENSP00000513153.1:p.Glu527Asp
ENST00000697165.1:c.1368A>T	ENSP00000513154.1:p.Glu456Asp
ENST00000347310.10:c.1671A>T MANE Select	ENSP00000321345.5:p.Glu557Asp
ENST00000637002.1:c.1062A>T	ENSP00000490340.1:p.Glu354Asp
ENST00000347310.9:c.1671A>T	ENSP00000321345.5:p.Glu557Asp
ENST00000395227.2:c.465A>T	ENSP00000378652.2:p.Glu155Asp
ENST00000425614.3:c.906A>T	ENSP00000387640.2:p.Glu302Asp
ENST00000473881.2:c.*497A>T	ENSP00000486667.1:n.*497A>T
NM_144701.2:c.1671A>T	NP_653302.2:p.Glu557Asp
XM_005270516.2:c.909A>T	XP_005270573.1:p.Glu303Asp
XM_011540789.1:c.1761A>T	XP_011539091.1:p.Glu587Asp
XM_011540790.1:c.1671A>T	XP_011539092.1:p.Glu557Asp
XM_011540791.1:c.1671A>T	XP_011539093.1:p.Glu557Asp
XM_011540790.3:c.1671A>T	XP_011539092.1:p.Glu557Asp
XM_011540791.3:c.1671A>T	XP_011539093.1:p.Glu557Asp
XR_001736993.1:n.1751A>T
NM_144701.3:c.1671A>T MANE Select	NP_653302.2:p.Glu557Asp