Canonical Allele Identifier: CA340729754

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724740T>A (hg19) ; chr1:g.67259057T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259057T>A , CM000663.2:g.67259057T>A	GRCh38
NC_000001.10:g.67724740T>A , CM000663.1:g.67724740T>A	GRCh37
NC_000001.9:g.67497328T>A	NCBI36
NG_011498.1:g.97572T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1658T>A	ENSP00000513138.1:n.1658T>A
ENST00000697150.1:c.1716T>A	ENSP00000513139.1:n.1716T>A
ENST00000697151.1:c.1649T>A	ENSP00000513140.1:n.1649T>A
ENST00000697164.1:c.1729T>A	ENSP00000513153.1:p.Ser577Thr
ENST00000697165.1:c.1516T>A	ENSP00000513154.1:p.Ser506Thr
ENST00000347310.10:c.1819T>A MANE Select	ENSP00000321345.5:p.Ser607Thr
ENST00000637002.1:c.1210T>A	ENSP00000490340.1:p.Ser404Thr
ENST00000347310.9:c.1819T>A	ENSP00000321345.5:p.Ser607Thr
ENST00000395227.2:c.613T>A	ENSP00000378652.2:p.Ser205Thr
ENST00000425614.3:c.1054T>A	ENSP00000387640.2:p.Ser352Thr
ENST00000473881.2:c.*645T>A	ENSP00000486667.1:n.*645T>A
NM_144701.2:c.1819T>A	NP_653302.2:p.Ser607Thr
XM_005270516.2:c.1057T>A	XP_005270573.1:p.Ser353Thr
XM_011540789.1:c.1909T>A	XP_011539091.1:p.Ser637Thr
XM_011540790.1:c.1819T>A	XP_011539092.1:p.Ser607Thr
XM_011540791.1:c.1819T>A	XP_011539093.1:p.Ser607Thr
XM_011540790.3:c.1819T>A	XP_011539092.1:p.Ser607Thr
XM_011540791.3:c.1819T>A	XP_011539093.1:p.Ser607Thr
XR_001736993.1:n.1899T>A
NM_144701.3:c.1819T>A MANE Select	NP_653302.2:p.Ser607Thr