Canonical Allele Identifier: CA340728722

Gene: IL23R

Linked Data

• COSMIC: COSM281900
• MyVariant Identifiers: chr1:g.67724483A>T (hg19) ; chr1:g.67258800A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258800A>T , CM000663.2:g.67258800A>T	GRCh38
NC_000001.10:g.67724483A>T , CM000663.1:g.67724483A>T	GRCh37
NC_000001.9:g.67497071A>T	NCBI36
NG_011498.1:g.97315A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1401A>T	ENSP00000513138.1:n.1401A>T
ENST00000697150.1:c.1459A>T	ENSP00000513139.1:n.1459A>T
ENST00000697151.1:c.1392A>T	ENSP00000513140.1:n.1392A>T
ENST00000697164.1:c.1472A>T	ENSP00000513153.1:p.Asn491Ile
ENST00000697165.1:c.1259A>T	ENSP00000513154.1:p.Asn420Ile
ENST00000347310.10:c.1562A>T MANE Select	ENSP00000321345.5:p.Asn521Ile
ENST00000637002.1:c.953A>T	ENSP00000490340.1:p.Asn318Ile
ENST00000347310.9:c.1562A>T	ENSP00000321345.5:p.Asn521Ile
ENST00000395227.2:c.356A>T	ENSP00000378652.2:p.Asn119Ile
ENST00000425614.3:c.797A>T	ENSP00000387640.2:p.Asn266Ile
ENST00000473881.2:c.*388A>T	ENSP00000486667.1:n.*388A>T
NM_144701.2:c.1562A>T	NP_653302.2:p.Asn521Ile
XM_005270516.2:c.800A>T	XP_005270573.1:p.Asn267Ile
XM_011540789.1:c.1652A>T	XP_011539091.1:p.Asn551Ile
XM_011540790.1:c.1562A>T	XP_011539092.1:p.Asn521Ile
XM_011540791.1:c.1562A>T	XP_011539093.1:p.Asn521Ile
XM_011540790.3:c.1562A>T	XP_011539092.1:p.Asn521Ile
XM_011540791.3:c.1562A>T	XP_011539093.1:p.Asn521Ile
XR_001736993.1:n.1642A>T
NM_144701.3:c.1562A>T MANE Select	NP_653302.2:p.Asn521Ile