Canonical Allele Identifier: CA418438575

Gene: IL23R

Linked Data

• gnomAD v4: 1-67258894-A-T
• COSMIC: COSM5676395
• MyVariant Identifiers: chr1:g.67724577A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258894A>T , CM000663.2:g.67258894A>T	GRCh38
NC_000001.10:g.67724577A>T , CM000663.1:g.67724577A>T	GRCh37
NC_000001.9:g.67497165A>T	NCBI36
NG_011498.1:g.97409A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1495A>T	ENSP00000513138.1:n.1495A>T
ENST00000697150.1:c.1553A>T	ENSP00000513139.1:n.1553A>T
ENST00000697151.1:c.1486A>T	ENSP00000513140.1:n.1486A>T
ENST00000697164.1:c.1566A>T	ENSP00000513153.1:p.Ile522=
ENST00000697165.1:c.1353A>T	ENSP00000513154.1:p.Ile451=
ENST00000347310.10:c.1656A>T MANE Select	ENSP00000321345.5:p.Ile552=
ENST00000637002.1:c.1047A>T	ENSP00000490340.1:p.Ile349=
ENST00000347310.9:c.1656A>T	ENSP00000321345.5:p.Ile552=
ENST00000395227.2:c.450A>T	ENSP00000378652.2:p.Ile150=
ENST00000425614.3:c.891A>T	ENSP00000387640.2:p.Ile297=
ENST00000473881.2:c.*482A>T	ENSP00000486667.1:n.*482A>T
NM_144701.2:c.1656A>T	NP_653302.2:p.Ile552=
XM_005270516.2:c.894A>T	XP_005270573.1:p.Ile298=
XM_011540789.1:c.1746A>T	XP_011539091.1:p.Ile582=
XM_011540790.1:c.1656A>T	XP_011539092.1:p.Ile552=
XM_011540791.1:c.1656A>T	XP_011539093.1:p.Ile552=
XM_011540790.3:c.1656A>T	XP_011539092.1:p.Ile552=
XM_011540791.3:c.1656A>T	XP_011539093.1:p.Ile552=
XR_001736993.1:n.1736A>T
NM_144701.3:c.1656A>T MANE Select	NP_653302.2:p.Ile552=