Canonical Allele Identifier: CA340725939

Gene: IL23R

Linked Data

• gnomAD v4: 1-67240275-G-T
• MyVariant Identifiers: chr1:g.67705958G>T (hg19) ; chr1:g.67240275G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67240275G>T , CM000663.2:g.67240275G>T	GRCh38
NC_000001.10:g.67705958G>T , CM000663.1:g.67705958G>T	GRCh37
NC_000001.9:g.67478546G>T	NCBI36
NG_011498.1:g.78790G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000697148.1:c.1018G>T	ENSP00000513137.1:n.1018G>T
ENST00000697149.1:c.981G>T	ENSP00000513138.1:n.981G>T
ENST00000697150.1:c.1045+3473G>T	ENSP00000513139.1:n.1045+3473G>T
ENST00000697151.1:c.1045+3473G>T	ENSP00000513140.1:n.1045+3473G>T
ENST00000697152.1:c.799-15562G>T	ENSP00000513141.1:n.799-15562G>T
ENST00000697153.1:c.795-15562G>T	ENSP00000513142.1:n.795-15562G>T
ENST00000697154.1:c.956-18203G>T	ENSP00000513143.1:n.956-18203G>T
ENST00000697155.1:c.649-18203G>T	ENSP00000513144.1:n.649-18203G>T
ENST00000697156.1:c.1142G>T	ENSP00000513145.1:p.Arg381Leu
ENST00000697157.1:c.996G>T	ENSP00000513146.1:n.996G>T
ENST00000697158.1:c.985G>T	ENSP00000513147.1:n.985G>T
ENST00000697159.1:c.835G>T	ENSP00000513148.1:n.835G>T
ENST00000697160.1:c.956-15562G>T	ENSP00000513149.1:n.956-15562G>T
ENST00000697161.1:c.678G>T	ENSP00000513150.1:n.678G>T
ENST00000697162.1:c.1071G>T	ENSP00000513151.1:n.1071G>T
ENST00000697163.1:c.1142G>T	ENSP00000513152.1:p.Arg381Leu
ENST00000697164.1:c.1052G>T	ENSP00000513153.1:p.Arg351Leu
ENST00000697165.1:c.839G>T	ENSP00000513154.1:p.Arg280Leu
ENST00000697223.1:c.891G>T	ENSP00000513190.1:n.891G>T
ENST00000697224.1:c.884+3473G>T	ENSP00000513191.1:n.884+3473G>T
ENST00000697225.1:c.745G>T	ENSP00000513192.1:n.745G>T
ENST00000697226.1:c.738+3473G>T	ENSP00000513193.1:n.738+3473G>T
ENST00000697227.1:c.978G>T	ENSP00000513194.1:n.978G>T
ENST00000697228.1:c.834G>T	ENSP00000513195.1:n.834G>T
ENST00000697229.1:c.885-15562G>T	ENSP00000513196.1:n.885-15562G>T
ENST00000697230.1:c.1052G>T	ENSP00000513197.1:p.Arg351Leu
ENST00000697231.1:c.1047G>T	ENSP00000513198.1:n.1047G>T
ENST00000697232.1:c.1071G>T	ENSP00000513199.1:n.1071G>T
ENST00000347310.10:c.1142G>T MANE Select	ENSP00000321345.5:p.Arg381Leu
ENST00000637002.1:c.533G>T	ENSP00000490340.1:p.Arg178Leu
ENST00000347310.9:c.1142G>T	ENSP00000321345.5:p.Arg381Leu
ENST00000395227.2:c.-58-15562G>T	ENSP00000378652.2:n.-58-15562G>T
ENST00000425614.3:c.377G>T	ENSP00000387640.2:p.Arg126Leu
ENST00000473881.2:c.191-15562G>T	ENSP00000486667.1:n.191-15562G>T
NM_144701.2:c.1142G>T	NP_653302.2:p.Arg381Leu
XM_005270516.2:c.380G>T	XP_005270573.1:p.Arg127Leu
XM_011540789.1:c.1232G>T	XP_011539091.1:p.Arg411Leu
XM_011540790.1:c.1142G>T	XP_011539092.1:p.Arg381Leu
XM_011540791.1:c.1142G>T	XP_011539093.1:p.Arg381Leu
XM_011540790.3:c.1142G>T	XP_011539092.1:p.Arg381Leu
XM_011540791.3:c.1142G>T	XP_011539093.1:p.Arg381Leu
XR_001736993.1:n.1228+3473G>T
NM_144701.3:c.1142G>T MANE Select	NP_653302.2:p.Arg381Leu