Canonical Allele Identifier: CA340729281

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724617T>A (hg19) ; chr1:g.67258934T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258934T>A , CM000663.2:g.67258934T>A	GRCh38
NC_000001.10:g.67724617T>A , CM000663.1:g.67724617T>A	GRCh37
NC_000001.9:g.67497205T>A	NCBI36
NG_011498.1:g.97449T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1535T>A	ENSP00000513138.1:n.1535T>A
ENST00000697150.1:c.1593T>A	ENSP00000513139.1:n.1593T>A
ENST00000697151.1:c.1526T>A	ENSP00000513140.1:n.1526T>A
ENST00000697164.1:c.1606T>A	ENSP00000513153.1:p.Ser536Thr
ENST00000697165.1:c.1393T>A	ENSP00000513154.1:p.Ser465Thr
ENST00000347310.10:c.1696T>A MANE Select	ENSP00000321345.5:p.Ser566Thr
ENST00000637002.1:c.1087T>A	ENSP00000490340.1:p.Ser363Thr
ENST00000347310.9:c.1696T>A	ENSP00000321345.5:p.Ser566Thr
ENST00000395227.2:c.490T>A	ENSP00000378652.2:p.Ser164Thr
ENST00000425614.3:c.931T>A	ENSP00000387640.2:p.Ser311Thr
ENST00000473881.2:c.*522T>A	ENSP00000486667.1:n.*522T>A
NM_144701.2:c.1696T>A	NP_653302.2:p.Ser566Thr
XM_005270516.2:c.934T>A	XP_005270573.1:p.Ser312Thr
XM_011540789.1:c.1786T>A	XP_011539091.1:p.Ser596Thr
XM_011540790.1:c.1696T>A	XP_011539092.1:p.Ser566Thr
XM_011540791.1:c.1696T>A	XP_011539093.1:p.Ser566Thr
XM_011540790.3:c.1696T>A	XP_011539092.1:p.Ser566Thr
XM_011540791.3:c.1696T>A	XP_011539093.1:p.Ser566Thr
XR_001736993.1:n.1776T>A
NM_144701.3:c.1696T>A MANE Select	NP_653302.2:p.Ser566Thr