Canonical Allele Identifier: CA418269016

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67705929T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67240246T>C , CM000663.2:g.67240246T>C	GRCh38
NC_000001.10:g.67705929T>C , CM000663.1:g.67705929T>C	GRCh37
NC_000001.9:g.67478517T>C	NCBI36
NG_011498.1:g.78761T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697148.1:c.989T>C	ENSP00000513137.1:n.989T>C
ENST00000697149.1:c.952T>C	ENSP00000513138.1:n.952T>C
ENST00000697150.1:c.1045+3444T>C	ENSP00000513139.1:n.1045+3444T>C
ENST00000697151.1:c.1045+3444T>C	ENSP00000513140.1:n.1045+3444T>C
ENST00000697152.1:c.799-15591T>C	ENSP00000513141.1:n.799-15591T>C
ENST00000697153.1:c.795-15591T>C	ENSP00000513142.1:n.795-15591T>C
ENST00000697154.1:c.956-18232T>C	ENSP00000513143.1:n.956-18232T>C
ENST00000697155.1:c.649-18232T>C	ENSP00000513144.1:n.649-18232T>C
ENST00000697156.1:c.1113T>C	ENSP00000513145.1:p.Ser371=
ENST00000697157.1:c.967T>C	ENSP00000513146.1:n.967T>C
ENST00000697158.1:c.956T>C	ENSP00000513147.1:n.956T>C
ENST00000697159.1:c.806T>C	ENSP00000513148.1:n.806T>C
ENST00000697160.1:c.956-15591T>C	ENSP00000513149.1:n.956-15591T>C
ENST00000697161.1:c.649T>C	ENSP00000513150.1:n.649T>C
ENST00000697162.1:c.1042T>C	ENSP00000513151.1:n.1042T>C
ENST00000697163.1:c.1113T>C	ENSP00000513152.1:p.Ser371=
ENST00000697164.1:c.1023T>C	ENSP00000513153.1:p.Ser341=
ENST00000697165.1:c.810T>C	ENSP00000513154.1:p.Ser270=
ENST00000697223.1:c.862T>C	ENSP00000513190.1:n.862T>C
ENST00000697224.1:c.884+3444T>C	ENSP00000513191.1:n.884+3444T>C
ENST00000697225.1:c.716T>C	ENSP00000513192.1:n.716T>C
ENST00000697226.1:c.738+3444T>C	ENSP00000513193.1:n.738+3444T>C
ENST00000697227.1:c.949T>C	ENSP00000513194.1:n.949T>C
ENST00000697228.1:c.805T>C	ENSP00000513195.1:n.805T>C
ENST00000697229.1:c.885-15591T>C	ENSP00000513196.1:n.885-15591T>C
ENST00000697230.1:c.1023T>C	ENSP00000513197.1:p.Ser341=
ENST00000697231.1:c.1018T>C	ENSP00000513198.1:n.1018T>C
ENST00000697232.1:c.1042T>C	ENSP00000513199.1:n.1042T>C
ENST00000347310.10:c.1113T>C MANE Select	ENSP00000321345.5:p.Ser371=
ENST00000637002.1:c.504T>C	ENSP00000490340.1:p.Ser168=
ENST00000347310.9:c.1113T>C	ENSP00000321345.5:p.Ser371=
ENST00000395227.2:c.-58-15591T>C	ENSP00000378652.2:n.-58-15591T>C
ENST00000425614.3:c.348T>C	ENSP00000387640.2:p.Ser116=
ENST00000473881.2:c.191-15591T>C	ENSP00000486667.1:n.191-15591T>C
NM_144701.2:c.1113T>C	NP_653302.2:p.Ser371=
XM_005270516.2:c.351T>C	XP_005270573.1:p.Ser117=
XM_011540789.1:c.1203T>C	XP_011539091.1:p.Ser401=
XM_011540790.1:c.1113T>C	XP_011539092.1:p.Ser371=
XM_011540791.1:c.1113T>C	XP_011539093.1:p.Ser371=
XM_011540790.3:c.1113T>C	XP_011539092.1:p.Ser371=
XM_011540791.3:c.1113T>C	XP_011539093.1:p.Ser371=
XR_001736993.1:n.1228+3444T>C
NM_144701.3:c.1113T>C MANE Select	NP_653302.2:p.Ser371=