Canonical Allele Identifier: CA418269033

Gene: IL23R

Linked Data

• dbSNP Id: rs368291075
• gnomAD v3: 1-67240274-C-A
• gnomAD v4: 1-67240274-C-A
• MyVariant Identifiers: chr1:g.67705957C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67240274C>A , CM000663.2:g.67240274C>A	GRCh38
NC_000001.10:g.67705957C>A , CM000663.1:g.67705957C>A	GRCh37
NC_000001.9:g.67478545C>A	NCBI36
NG_011498.1:g.78789C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697148.1:c.1017C>A	ENSP00000513137.1:n.1017C>A
ENST00000697149.1:c.980C>A	ENSP00000513138.1:n.980C>A
ENST00000697150.1:c.1045+3472C>A	ENSP00000513139.1:n.1045+3472C>A
ENST00000697151.1:c.1045+3472C>A	ENSP00000513140.1:n.1045+3472C>A
ENST00000697152.1:c.799-15563C>A	ENSP00000513141.1:n.799-15563C>A
ENST00000697153.1:c.795-15563C>A	ENSP00000513142.1:n.795-15563C>A
ENST00000697154.1:c.956-18204C>A	ENSP00000513143.1:n.956-18204C>A
ENST00000697155.1:c.649-18204C>A	ENSP00000513144.1:n.649-18204C>A
ENST00000697156.1:c.1141C>A	ENSP00000513145.1:p.Arg381=
ENST00000697157.1:c.995C>A	ENSP00000513146.1:n.995C>A
ENST00000697158.1:c.984C>A	ENSP00000513147.1:n.984C>A
ENST00000697159.1:c.834C>A	ENSP00000513148.1:n.834C>A
ENST00000697160.1:c.956-15563C>A	ENSP00000513149.1:n.956-15563C>A
ENST00000697161.1:c.677C>A	ENSP00000513150.1:n.677C>A
ENST00000697162.1:c.1070C>A	ENSP00000513151.1:n.1070C>A
ENST00000697163.1:c.1141C>A	ENSP00000513152.1:p.Arg381=
ENST00000697164.1:c.1051C>A	ENSP00000513153.1:p.Arg351=
ENST00000697165.1:c.838C>A	ENSP00000513154.1:p.Arg280=
ENST00000697223.1:c.890C>A	ENSP00000513190.1:n.890C>A
ENST00000697224.1:c.884+3472C>A	ENSP00000513191.1:n.884+3472C>A
ENST00000697225.1:c.744C>A	ENSP00000513192.1:n.744C>A
ENST00000697226.1:c.738+3472C>A	ENSP00000513193.1:n.738+3472C>A
ENST00000697227.1:c.977C>A	ENSP00000513194.1:n.977C>A
ENST00000697228.1:c.833C>A	ENSP00000513195.1:n.833C>A
ENST00000697229.1:c.885-15563C>A	ENSP00000513196.1:n.885-15563C>A
ENST00000697230.1:c.1051C>A	ENSP00000513197.1:p.Arg351=
ENST00000697231.1:c.1046C>A	ENSP00000513198.1:n.1046C>A
ENST00000697232.1:c.1070C>A	ENSP00000513199.1:n.1070C>A
ENST00000347310.10:c.1141C>A MANE Select	ENSP00000321345.5:p.Arg381=
ENST00000637002.1:c.532C>A	ENSP00000490340.1:p.Arg178=
ENST00000347310.9:c.1141C>A	ENSP00000321345.5:p.Arg381=
ENST00000395227.2:c.-58-15563C>A	ENSP00000378652.2:n.-58-15563C>A
ENST00000425614.3:c.376C>A	ENSP00000387640.2:p.Arg126=
ENST00000473881.2:c.191-15563C>A	ENSP00000486667.1:n.191-15563C>A
NM_144701.2:c.1141C>A	NP_653302.2:p.Arg381=
XM_005270516.2:c.379C>A	XP_005270573.1:p.Arg127=
XM_011540789.1:c.1231C>A	XP_011539091.1:p.Arg411=
XM_011540790.1:c.1141C>A	XP_011539092.1:p.Arg381=
XM_011540791.1:c.1141C>A	XP_011539093.1:p.Arg381=
XM_011540790.3:c.1141C>A	XP_011539092.1:p.Arg381=
XM_011540791.3:c.1141C>A	XP_011539093.1:p.Arg381=
XR_001736993.1:n.1228+3472C>A
NM_144701.3:c.1141C>A MANE Select	NP_653302.2:p.Arg381=