Canonical Allele Identifier: CA340725931

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67705954T>G (hg19) ; chr1:g.67240271T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67240271T>G , CM000663.2:g.67240271T>G	GRCh38
NC_000001.10:g.67705954T>G , CM000663.1:g.67705954T>G	GRCh37
NC_000001.9:g.67478542T>G	NCBI36
NG_011498.1:g.78786T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697148.1:c.1014T>G	ENSP00000513137.1:n.1014T>G
ENST00000697149.1:c.977T>G	ENSP00000513138.1:n.977T>G
ENST00000697150.1:c.1045+3469T>G	ENSP00000513139.1:n.1045+3469T>G
ENST00000697151.1:c.1045+3469T>G	ENSP00000513140.1:n.1045+3469T>G
ENST00000697152.1:c.799-15566T>G	ENSP00000513141.1:n.799-15566T>G
ENST00000697153.1:c.795-15566T>G	ENSP00000513142.1:n.795-15566T>G
ENST00000697154.1:c.956-18207T>G	ENSP00000513143.1:n.956-18207T>G
ENST00000697155.1:c.649-18207T>G	ENSP00000513144.1:n.649-18207T>G
ENST00000697156.1:c.1138T>G	ENSP00000513145.1:p.Phe380Val
ENST00000697157.1:c.992T>G	ENSP00000513146.1:n.992T>G
ENST00000697158.1:c.981T>G	ENSP00000513147.1:n.981T>G
ENST00000697159.1:c.831T>G	ENSP00000513148.1:n.831T>G
ENST00000697160.1:c.956-15566T>G	ENSP00000513149.1:n.956-15566T>G
ENST00000697161.1:c.674T>G	ENSP00000513150.1:n.674T>G
ENST00000697162.1:c.1067T>G	ENSP00000513151.1:n.1067T>G
ENST00000697163.1:c.1138T>G	ENSP00000513152.1:p.Phe380Val
ENST00000697164.1:c.1048T>G	ENSP00000513153.1:p.Phe350Val
ENST00000697165.1:c.835T>G	ENSP00000513154.1:p.Phe279Val
ENST00000697223.1:c.887T>G	ENSP00000513190.1:n.887T>G
ENST00000697224.1:c.884+3469T>G	ENSP00000513191.1:n.884+3469T>G
ENST00000697225.1:c.741T>G	ENSP00000513192.1:n.741T>G
ENST00000697226.1:c.738+3469T>G	ENSP00000513193.1:n.738+3469T>G
ENST00000697227.1:c.974T>G	ENSP00000513194.1:n.974T>G
ENST00000697228.1:c.830T>G	ENSP00000513195.1:n.830T>G
ENST00000697229.1:c.885-15566T>G	ENSP00000513196.1:n.885-15566T>G
ENST00000697230.1:c.1048T>G	ENSP00000513197.1:p.Phe350Val
ENST00000697231.1:c.1043T>G	ENSP00000513198.1:n.1043T>G
ENST00000697232.1:c.1067T>G	ENSP00000513199.1:n.1067T>G
ENST00000347310.10:c.1138T>G MANE Select	ENSP00000321345.5:p.Phe380Val
ENST00000637002.1:c.529T>G	ENSP00000490340.1:p.Phe177Val
ENST00000347310.9:c.1138T>G	ENSP00000321345.5:p.Phe380Val
ENST00000395227.2:c.-58-15566T>G	ENSP00000378652.2:n.-58-15566T>G
ENST00000425614.3:c.373T>G	ENSP00000387640.2:p.Phe125Val
ENST00000473881.2:c.191-15566T>G	ENSP00000486667.1:n.191-15566T>G
NM_144701.2:c.1138T>G	NP_653302.2:p.Phe380Val
XM_005270516.2:c.376T>G	XP_005270573.1:p.Phe126Val
XM_011540789.1:c.1228T>G	XP_011539091.1:p.Phe410Val
XM_011540790.1:c.1138T>G	XP_011539092.1:p.Phe380Val
XM_011540791.1:c.1138T>G	XP_011539093.1:p.Phe380Val
XM_011540790.3:c.1138T>G	XP_011539092.1:p.Phe380Val
XM_011540791.3:c.1138T>G	XP_011539093.1:p.Phe380Val
XR_001736993.1:n.1228+3469T>G
NM_144701.3:c.1138T>G MANE Select	NP_653302.2:p.Phe380Val