Canonical Allele Identifier: CA340728640

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724444C>A (hg19) ; chr1:g.67258761C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258761C>A , CM000663.2:g.67258761C>A	GRCh38
NC_000001.10:g.67724444C>A , CM000663.1:g.67724444C>A	GRCh37
NC_000001.9:g.67497032C>A	NCBI36
NG_011498.1:g.97276C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1362C>A	ENSP00000513138.1:n.1362C>A
ENST00000697150.1:c.1420C>A	ENSP00000513139.1:n.1420C>A
ENST00000697151.1:c.1353C>A	ENSP00000513140.1:n.1353C>A
ENST00000697164.1:c.1433C>A	ENSP00000513153.1:p.Thr478Lys
ENST00000697165.1:c.1220C>A	ENSP00000513154.1:p.Thr407Lys
ENST00000347310.10:c.1523C>A MANE Select	ENSP00000321345.5:p.Thr508Lys
ENST00000637002.1:c.914C>A	ENSP00000490340.1:p.Thr305Lys
ENST00000347310.9:c.1523C>A	ENSP00000321345.5:p.Thr508Lys
ENST00000395227.2:c.317C>A	ENSP00000378652.2:p.Thr106Lys
ENST00000425614.3:c.758C>A	ENSP00000387640.2:p.Thr253Lys
ENST00000473881.2:c.*349C>A	ENSP00000486667.1:n.*349C>A
NM_144701.2:c.1523C>A	NP_653302.2:p.Thr508Lys
XM_005270516.2:c.761C>A	XP_005270573.1:p.Thr254Lys
XM_011540789.1:c.1613C>A	XP_011539091.1:p.Thr538Lys
XM_011540790.1:c.1523C>A	XP_011539092.1:p.Thr508Lys
XM_011540791.1:c.1523C>A	XP_011539093.1:p.Thr508Lys
XM_011540790.3:c.1523C>A	XP_011539092.1:p.Thr508Lys
XM_011540791.3:c.1523C>A	XP_011539093.1:p.Thr508Lys
XR_001736993.1:n.1603C>A
NM_144701.3:c.1523C>A MANE Select	NP_653302.2:p.Thr508Lys