Canonical Allele Identifier: CA340728864

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724536T>A (hg19) ; chr1:g.67258853T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258853T>A , CM000663.2:g.67258853T>A	GRCh38
NC_000001.10:g.67724536T>A , CM000663.1:g.67724536T>A	GRCh37
NC_000001.9:g.67497124T>A	NCBI36
NG_011498.1:g.97368T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1454T>A	ENSP00000513138.1:n.1454T>A
ENST00000697150.1:c.1512T>A	ENSP00000513139.1:n.1512T>A
ENST00000697151.1:c.1445T>A	ENSP00000513140.1:n.1445T>A
ENST00000697164.1:c.1525T>A	ENSP00000513153.1:p.Ser509Thr
ENST00000697165.1:c.1312T>A	ENSP00000513154.1:p.Ser438Thr
ENST00000347310.10:c.1615T>A MANE Select	ENSP00000321345.5:p.Ser539Thr
ENST00000637002.1:c.1006T>A	ENSP00000490340.1:p.Ser336Thr
ENST00000347310.9:c.1615T>A	ENSP00000321345.5:p.Ser539Thr
ENST00000395227.2:c.409T>A	ENSP00000378652.2:p.Ser137Thr
ENST00000425614.3:c.850T>A	ENSP00000387640.2:p.Ser284Thr
ENST00000473881.2:c.*441T>A	ENSP00000486667.1:n.*441T>A
NM_144701.2:c.1615T>A	NP_653302.2:p.Ser539Thr
XM_005270516.2:c.853T>A	XP_005270573.1:p.Ser285Thr
XM_011540789.1:c.1705T>A	XP_011539091.1:p.Ser569Thr
XM_011540790.1:c.1615T>A	XP_011539092.1:p.Ser539Thr
XM_011540791.1:c.1615T>A	XP_011539093.1:p.Ser539Thr
XM_011540790.3:c.1615T>A	XP_011539092.1:p.Ser539Thr
XM_011540791.3:c.1615T>A	XP_011539093.1:p.Ser539Thr
XR_001736993.1:n.1695T>A
NM_144701.3:c.1615T>A MANE Select	NP_653302.2:p.Ser539Thr