Canonical Allele Identifier: CA340728642

Gene: IL23R

Linked Data

• gnomAD v4: 1-67258761-C-T
• MyVariant Identifiers: chr1:g.67724444C>T (hg19) ; chr1:g.67258761C>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1362C>T	ENSP00000513138.1:n.1362C>T
ENST00000697150.1:c.1420C>T	ENSP00000513139.1:n.1420C>T
ENST00000697151.1:c.1353C>T	ENSP00000513140.1:n.1353C>T
ENST00000697164.1:c.1433C>T	ENSP00000513153.1:p.Thr478Ile
ENST00000697165.1:c.1220C>T	ENSP00000513154.1:p.Thr407Ile
ENST00000347310.10:c.1523C>T MANE Select	ENSP00000321345.5:p.Thr508Ile
ENST00000637002.1:c.914C>T	ENSP00000490340.1:p.Thr305Ile
ENST00000347310.9:c.1523C>T	ENSP00000321345.5:p.Thr508Ile
ENST00000395227.2:c.317C>T	ENSP00000378652.2:p.Thr106Ile
ENST00000425614.3:c.758C>T	ENSP00000387640.2:p.Thr253Ile
ENST00000473881.2:c.*349C>T	ENSP00000486667.1:n.*349C>T
NM_144701.2:c.1523C>T	NP_653302.2:p.Thr508Ile
XM_005270516.2:c.761C>T	XP_005270573.1:p.Thr254Ile
XM_011540789.1:c.1613C>T	XP_011539091.1:p.Thr538Ile
XM_011540790.1:c.1523C>T	XP_011539092.1:p.Thr508Ile
XM_011540791.1:c.1523C>T	XP_011539093.1:p.Thr508Ile
XM_011540790.3:c.1523C>T	XP_011539092.1:p.Thr508Ile
XM_011540791.3:c.1523C>T	XP_011539093.1:p.Thr508Ile
XR_001736993.1:n.1603C>T
NM_144701.3:c.1523C>T MANE Select	NP_653302.2:p.Thr508Ile