Canonical Allele Identifier: CA340725862

Gene: IL23R

Linked Data

• gnomAD v4: 1-67240239-T-C
• MyVariant Identifiers: chr1:g.67705922T>C (hg19) ; chr1:g.67240239T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67240239T>C , CM000663.2:g.67240239T>C	GRCh38
NC_000001.10:g.67705922T>C , CM000663.1:g.67705922T>C	GRCh37
NC_000001.9:g.67478510T>C	NCBI36
NG_011498.1:g.78754T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697148.1:c.982T>C	ENSP00000513137.1:n.982T>C
ENST00000697149.1:c.945T>C	ENSP00000513138.1:n.945T>C
ENST00000697150.1:c.1045+3437T>C	ENSP00000513139.1:n.1045+3437T>C
ENST00000697151.1:c.1045+3437T>C	ENSP00000513140.1:n.1045+3437T>C
ENST00000697152.1:c.799-15598T>C	ENSP00000513141.1:n.799-15598T>C
ENST00000697153.1:c.795-15598T>C	ENSP00000513142.1:n.795-15598T>C
ENST00000697154.1:c.956-18239T>C	ENSP00000513143.1:n.956-18239T>C
ENST00000697155.1:c.649-18239T>C	ENSP00000513144.1:n.649-18239T>C
ENST00000697156.1:c.1106T>C	ENSP00000513145.1:p.Ile369Thr
ENST00000697157.1:c.960T>C	ENSP00000513146.1:n.960T>C
ENST00000697158.1:c.949T>C	ENSP00000513147.1:n.949T>C
ENST00000697159.1:c.799T>C	ENSP00000513148.1:n.799T>C
ENST00000697160.1:c.956-15598T>C	ENSP00000513149.1:n.956-15598T>C
ENST00000697161.1:c.642T>C	ENSP00000513150.1:n.642T>C
ENST00000697162.1:c.1035T>C	ENSP00000513151.1:n.1035T>C
ENST00000697163.1:c.1106T>C	ENSP00000513152.1:p.Ile369Thr
ENST00000697164.1:c.1016T>C	ENSP00000513153.1:p.Ile339Thr
ENST00000697165.1:c.803T>C	ENSP00000513154.1:p.Ile268Thr
ENST00000697223.1:c.855T>C	ENSP00000513190.1:n.855T>C
ENST00000697224.1:c.884+3437T>C	ENSP00000513191.1:n.884+3437T>C
ENST00000697225.1:c.709T>C	ENSP00000513192.1:n.709T>C
ENST00000697226.1:c.738+3437T>C	ENSP00000513193.1:n.738+3437T>C
ENST00000697227.1:c.942T>C	ENSP00000513194.1:n.942T>C
ENST00000697228.1:c.798T>C	ENSP00000513195.1:n.798T>C
ENST00000697229.1:c.885-15598T>C	ENSP00000513196.1:n.885-15598T>C
ENST00000697230.1:c.1016T>C	ENSP00000513197.1:p.Ile339Thr
ENST00000697231.1:c.1011T>C	ENSP00000513198.1:n.1011T>C
ENST00000697232.1:c.1035T>C	ENSP00000513199.1:n.1035T>C
ENST00000347310.10:c.1106T>C MANE Select	ENSP00000321345.5:p.Ile369Thr
ENST00000637002.1:c.497T>C	ENSP00000490340.1:p.Ile166Thr
ENST00000347310.9:c.1106T>C	ENSP00000321345.5:p.Ile369Thr
ENST00000395227.2:c.-58-15598T>C	ENSP00000378652.2:n.-58-15598T>C
ENST00000425614.3:c.341T>C	ENSP00000387640.2:p.Ile114Thr
ENST00000473881.2:c.191-15598T>C	ENSP00000486667.1:n.191-15598T>C
NM_144701.2:c.1106T>C	NP_653302.2:p.Ile369Thr
XM_005270516.2:c.344T>C	XP_005270573.1:p.Ile115Thr
XM_011540789.1:c.1196T>C	XP_011539091.1:p.Ile399Thr
XM_011540790.1:c.1106T>C	XP_011539092.1:p.Ile369Thr
XM_011540791.1:c.1106T>C	XP_011539093.1:p.Ile369Thr
XM_011540790.3:c.1106T>C	XP_011539092.1:p.Ile369Thr
XM_011540791.3:c.1106T>C	XP_011539093.1:p.Ile369Thr
XR_001736993.1:n.1228+3437T>C
NM_144701.3:c.1106T>C MANE Select	NP_653302.2:p.Ile369Thr