Canonical Allele Identifier: CA340725898

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67705940T>C (hg19) ; chr1:g.67240257T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67240257T>C , CM000663.2:g.67240257T>C	GRCh38
NC_000001.10:g.67705940T>C , CM000663.1:g.67705940T>C	GRCh37
NC_000001.9:g.67478528T>C	NCBI36
NG_011498.1:g.78772T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697148.1:c.1000T>C	ENSP00000513137.1:n.1000T>C
ENST00000697149.1:c.963T>C	ENSP00000513138.1:n.963T>C
ENST00000697150.1:c.1045+3455T>C	ENSP00000513139.1:n.1045+3455T>C
ENST00000697151.1:c.1045+3455T>C	ENSP00000513140.1:n.1045+3455T>C
ENST00000697152.1:c.799-15580T>C	ENSP00000513141.1:n.799-15580T>C
ENST00000697153.1:c.795-15580T>C	ENSP00000513142.1:n.795-15580T>C
ENST00000697154.1:c.956-18221T>C	ENSP00000513143.1:n.956-18221T>C
ENST00000697155.1:c.649-18221T>C	ENSP00000513144.1:n.649-18221T>C
ENST00000697156.1:c.1124T>C	ENSP00000513145.1:p.Ile375Thr
ENST00000697157.1:c.978T>C	ENSP00000513146.1:n.978T>C
ENST00000697158.1:c.967T>C	ENSP00000513147.1:n.967T>C
ENST00000697159.1:c.817T>C	ENSP00000513148.1:n.817T>C
ENST00000697160.1:c.956-15580T>C	ENSP00000513149.1:n.956-15580T>C
ENST00000697161.1:c.660T>C	ENSP00000513150.1:n.660T>C
ENST00000697162.1:c.1053T>C	ENSP00000513151.1:n.1053T>C
ENST00000697163.1:c.1124T>C	ENSP00000513152.1:p.Ile375Thr
ENST00000697164.1:c.1034T>C	ENSP00000513153.1:p.Ile345Thr
ENST00000697165.1:c.821T>C	ENSP00000513154.1:p.Ile274Thr
ENST00000697223.1:c.873T>C	ENSP00000513190.1:n.873T>C
ENST00000697224.1:c.884+3455T>C	ENSP00000513191.1:n.884+3455T>C
ENST00000697225.1:c.727T>C	ENSP00000513192.1:n.727T>C
ENST00000697226.1:c.738+3455T>C	ENSP00000513193.1:n.738+3455T>C
ENST00000697227.1:c.960T>C	ENSP00000513194.1:n.960T>C
ENST00000697228.1:c.816T>C	ENSP00000513195.1:n.816T>C
ENST00000697229.1:c.885-15580T>C	ENSP00000513196.1:n.885-15580T>C
ENST00000697230.1:c.1034T>C	ENSP00000513197.1:p.Ile345Thr
ENST00000697231.1:c.1029T>C	ENSP00000513198.1:n.1029T>C
ENST00000697232.1:c.1053T>C	ENSP00000513199.1:n.1053T>C
ENST00000347310.10:c.1124T>C MANE Select	ENSP00000321345.5:p.Ile375Thr
ENST00000637002.1:c.515T>C	ENSP00000490340.1:p.Ile172Thr
ENST00000347310.9:c.1124T>C	ENSP00000321345.5:p.Ile375Thr
ENST00000395227.2:c.-58-15580T>C	ENSP00000378652.2:n.-58-15580T>C
ENST00000425614.3:c.359T>C	ENSP00000387640.2:p.Ile120Thr
ENST00000473881.2:c.191-15580T>C	ENSP00000486667.1:n.191-15580T>C
NM_144701.2:c.1124T>C	NP_653302.2:p.Ile375Thr
XM_005270516.2:c.362T>C	XP_005270573.1:p.Ile121Thr
XM_011540789.1:c.1214T>C	XP_011539091.1:p.Ile405Thr
XM_011540790.1:c.1124T>C	XP_011539092.1:p.Ile375Thr
XM_011540791.1:c.1124T>C	XP_011539093.1:p.Ile375Thr
XM_011540790.3:c.1124T>C	XP_011539092.1:p.Ile375Thr
XM_011540791.3:c.1124T>C	XP_011539093.1:p.Ile375Thr
XR_001736993.1:n.1228+3455T>C
NM_144701.3:c.1124T>C MANE Select	NP_653302.2:p.Ile375Thr