Canonical Allele Identifier: CA418268973

Gene: IL23R

Linked Data

• gnomAD v4: 1-67240180-C-T
• MyVariant Identifiers: chr1:g.67705863C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67240180C>T , CM000663.2:g.67240180C>T	GRCh38
NC_000001.10:g.67705863C>T , CM000663.1:g.67705863C>T	GRCh37
NC_000001.9:g.67478451C>T	NCBI36
NG_011498.1:g.78695C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000697148.1:c.923C>T	ENSP00000513137.1:n.923C>T
ENST00000697149.1:c.886C>T	ENSP00000513138.1:n.886C>T
ENST00000697150.1:c.1045+3378C>T	ENSP00000513139.1:n.1045+3378C>T
ENST00000697151.1:c.1045+3378C>T	ENSP00000513140.1:n.1045+3378C>T
ENST00000697152.1:c.799-15657C>T	ENSP00000513141.1:n.799-15657C>T
ENST00000697153.1:c.795-15657C>T	ENSP00000513142.1:n.795-15657C>T
ENST00000697154.1:c.956-18298C>T	ENSP00000513143.1:n.956-18298C>T
ENST00000697155.1:c.649-18298C>T	ENSP00000513144.1:n.649-18298C>T
ENST00000697156.1:c.1047C>T	ENSP00000513145.1:p.Asp349=
ENST00000697157.1:c.901C>T	ENSP00000513146.1:n.901C>T
ENST00000697158.1:c.890C>T	ENSP00000513147.1:n.890C>T
ENST00000697159.1:c.740C>T	ENSP00000513148.1:n.740C>T
ENST00000697160.1:c.956-15657C>T	ENSP00000513149.1:n.956-15657C>T
ENST00000697161.1:c.583C>T	ENSP00000513150.1:n.583C>T
ENST00000697162.1:c.976C>T	ENSP00000513151.1:n.976C>T
ENST00000697163.1:c.1047C>T	ENSP00000513152.1:p.Asp349=
ENST00000697164.1:c.957C>T	ENSP00000513153.1:p.Asp319=
ENST00000697165.1:c.744C>T	ENSP00000513154.1:p.Asp248=
ENST00000697223.1:c.796C>T	ENSP00000513190.1:n.796C>T
ENST00000697224.1:c.884+3378C>T	ENSP00000513191.1:n.884+3378C>T
ENST00000697225.1:c.650C>T	ENSP00000513192.1:n.650C>T
ENST00000697226.1:c.738+3378C>T	ENSP00000513193.1:n.738+3378C>T
ENST00000697227.1:c.883C>T	ENSP00000513194.1:n.883C>T
ENST00000697228.1:c.739C>T	ENSP00000513195.1:n.739C>T
ENST00000697229.1:c.885-15657C>T	ENSP00000513196.1:n.885-15657C>T
ENST00000697230.1:c.957C>T	ENSP00000513197.1:p.Asp319=
ENST00000697231.1:c.952C>T	ENSP00000513198.1:n.952C>T
ENST00000697232.1:c.976C>T	ENSP00000513199.1:n.976C>T
ENST00000347310.10:c.1047C>T MANE Select	ENSP00000321345.5:p.Asp349=
ENST00000637002.1:c.438C>T	ENSP00000490340.1:p.Asp146=
ENST00000347310.9:c.1047C>T	ENSP00000321345.5:p.Asp349=
ENST00000395227.2:c.-58-15657C>T	ENSP00000378652.2:n.-58-15657C>T
ENST00000425614.3:c.282C>T	ENSP00000387640.2:p.Asp94=
ENST00000473881.2:c.191-15657C>T	ENSP00000486667.1:n.191-15657C>T
NM_144701.2:c.1047C>T	NP_653302.2:p.Asp349=
XM_005270516.2:c.285C>T	XP_005270573.1:p.Asp95=
XM_011540789.1:c.1137C>T	XP_011539091.1:p.Asp379=
XM_011540790.1:c.1047C>T	XP_011539092.1:p.Asp349=
XM_011540791.1:c.1047C>T	XP_011539093.1:p.Asp349=
XM_011540790.3:c.1047C>T	XP_011539092.1:p.Asp349=
XM_011540791.3:c.1047C>T	XP_011539093.1:p.Asp349=
XR_001736993.1:n.1228+3378C>T
NM_144701.3:c.1047C>T MANE Select	NP_653302.2:p.Asp349=