Canonical Allele Identifier: CA340725853

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67705918T>A (hg19) ; chr1:g.67240235T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67240235T>A , CM000663.2:g.67240235T>A	GRCh38
NC_000001.10:g.67705918T>A , CM000663.1:g.67705918T>A	GRCh37
NC_000001.9:g.67478506T>A	NCBI36
NG_011498.1:g.78750T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697148.1:c.978T>A	ENSP00000513137.1:n.978T>A
ENST00000697149.1:c.941T>A	ENSP00000513138.1:n.941T>A
ENST00000697150.1:c.1045+3433T>A	ENSP00000513139.1:n.1045+3433T>A
ENST00000697151.1:c.1045+3433T>A	ENSP00000513140.1:n.1045+3433T>A
ENST00000697152.1:c.799-15602T>A	ENSP00000513141.1:n.799-15602T>A
ENST00000697153.1:c.795-15602T>A	ENSP00000513142.1:n.795-15602T>A
ENST00000697154.1:c.956-18243T>A	ENSP00000513143.1:n.956-18243T>A
ENST00000697155.1:c.649-18243T>A	ENSP00000513144.1:n.649-18243T>A
ENST00000697156.1:c.1102T>A	ENSP00000513145.1:p.Ser368Thr
ENST00000697157.1:c.956T>A	ENSP00000513146.1:n.956T>A
ENST00000697158.1:c.945T>A	ENSP00000513147.1:n.945T>A
ENST00000697159.1:c.795T>A	ENSP00000513148.1:n.795T>A
ENST00000697160.1:c.956-15602T>A	ENSP00000513149.1:n.956-15602T>A
ENST00000697161.1:c.638T>A	ENSP00000513150.1:n.638T>A
ENST00000697162.1:c.1031T>A	ENSP00000513151.1:n.1031T>A
ENST00000697163.1:c.1102T>A	ENSP00000513152.1:p.Ser368Thr
ENST00000697164.1:c.1012T>A	ENSP00000513153.1:p.Ser338Thr
ENST00000697165.1:c.799T>A	ENSP00000513154.1:p.Ser267Thr
ENST00000697223.1:c.851T>A	ENSP00000513190.1:n.851T>A
ENST00000697224.1:c.884+3433T>A	ENSP00000513191.1:n.884+3433T>A
ENST00000697225.1:c.705T>A	ENSP00000513192.1:n.705T>A
ENST00000697226.1:c.738+3433T>A	ENSP00000513193.1:n.738+3433T>A
ENST00000697227.1:c.938T>A	ENSP00000513194.1:n.938T>A
ENST00000697228.1:c.794T>A	ENSP00000513195.1:n.794T>A
ENST00000697229.1:c.885-15602T>A	ENSP00000513196.1:n.885-15602T>A
ENST00000697230.1:c.1012T>A	ENSP00000513197.1:p.Ser338Thr
ENST00000697231.1:c.1007T>A	ENSP00000513198.1:n.1007T>A
ENST00000697232.1:c.1031T>A	ENSP00000513199.1:n.1031T>A
ENST00000347310.10:c.1102T>A MANE Select	ENSP00000321345.5:p.Ser368Thr
ENST00000637002.1:c.493T>A	ENSP00000490340.1:p.Ser165Thr
ENST00000347310.9:c.1102T>A	ENSP00000321345.5:p.Ser368Thr
ENST00000395227.2:c.-58-15602T>A	ENSP00000378652.2:n.-58-15602T>A
ENST00000425614.3:c.337T>A	ENSP00000387640.2:p.Ser113Thr
ENST00000473881.2:c.191-15602T>A	ENSP00000486667.1:n.191-15602T>A
NM_144701.2:c.1102T>A	NP_653302.2:p.Ser368Thr
XM_005270516.2:c.340T>A	XP_005270573.1:p.Ser114Thr
XM_011540789.1:c.1192T>A	XP_011539091.1:p.Ser398Thr
XM_011540790.1:c.1102T>A	XP_011539092.1:p.Ser368Thr
XM_011540791.1:c.1102T>A	XP_011539093.1:p.Ser368Thr
XM_011540790.3:c.1102T>A	XP_011539092.1:p.Ser368Thr
XM_011540791.3:c.1102T>A	XP_011539093.1:p.Ser368Thr
XR_001736993.1:n.1228+3433T>A
NM_144701.3:c.1102T>A MANE Select	NP_653302.2:p.Ser368Thr