Canonical Allele Identifier: CA418438652

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724637C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258954C>T , CM000663.2:g.67258954C>T	GRCh38
NC_000001.10:g.67724637C>T , CM000663.1:g.67724637C>T	GRCh37
NC_000001.9:g.67497225C>T	NCBI36
NG_011498.1:g.97469C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1555C>T	ENSP00000513138.1:n.1555C>T
ENST00000697150.1:c.1613C>T	ENSP00000513139.1:n.1613C>T
ENST00000697151.1:c.1546C>T	ENSP00000513140.1:n.1546C>T
ENST00000697164.1:c.1626C>T	ENSP00000513153.1:p.Thr542=
ENST00000697165.1:c.1413C>T	ENSP00000513154.1:p.Thr471=
ENST00000347310.10:c.1716C>T MANE Select	ENSP00000321345.5:p.Thr572=
ENST00000637002.1:c.1107C>T	ENSP00000490340.1:p.Thr369=
ENST00000347310.9:c.1716C>T	ENSP00000321345.5:p.Thr572=
ENST00000395227.2:c.510C>T	ENSP00000378652.2:p.Thr170=
ENST00000425614.3:c.951C>T	ENSP00000387640.2:p.Thr317=
ENST00000473881.2:c.*542C>T	ENSP00000486667.1:n.*542C>T
NM_144701.2:c.1716C>T	NP_653302.2:p.Thr572=
XM_005270516.2:c.954C>T	XP_005270573.1:p.Thr318=
XM_011540789.1:c.1806C>T	XP_011539091.1:p.Thr602=
XM_011540790.1:c.1716C>T	XP_011539092.1:p.Thr572=
XM_011540791.1:c.1716C>T	XP_011539093.1:p.Thr572=
XM_011540790.3:c.1716C>T	XP_011539092.1:p.Thr572=
XM_011540791.3:c.1716C>T	XP_011539093.1:p.Thr572=
XR_001736993.1:n.1796C>T
NM_144701.3:c.1716C>T MANE Select	NP_653302.2:p.Thr572=