Canonical Allele Identifier: CA340725753

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67705871G>T (hg19) ; chr1:g.67240188G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67240188G>T , CM000663.2:g.67240188G>T	GRCh38
NC_000001.10:g.67705871G>T , CM000663.1:g.67705871G>T	GRCh37
NC_000001.9:g.67478459G>T	NCBI36
NG_011498.1:g.78703G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000697148.1:c.931G>T	ENSP00000513137.1:n.931G>T
ENST00000697149.1:c.894G>T	ENSP00000513138.1:n.894G>T
ENST00000697150.1:c.1045+3386G>T	ENSP00000513139.1:n.1045+3386G>T
ENST00000697151.1:c.1045+3386G>T	ENSP00000513140.1:n.1045+3386G>T
ENST00000697152.1:c.799-15649G>T	ENSP00000513141.1:n.799-15649G>T
ENST00000697153.1:c.795-15649G>T	ENSP00000513142.1:n.795-15649G>T
ENST00000697154.1:c.956-18290G>T	ENSP00000513143.1:n.956-18290G>T
ENST00000697155.1:c.649-18290G>T	ENSP00000513144.1:n.649-18290G>T
ENST00000697156.1:c.1055G>T	ENSP00000513145.1:p.Gly352Val
ENST00000697157.1:c.909G>T	ENSP00000513146.1:n.909G>T
ENST00000697158.1:c.898G>T	ENSP00000513147.1:n.898G>T
ENST00000697159.1:c.748G>T	ENSP00000513148.1:n.748G>T
ENST00000697160.1:c.956-15649G>T	ENSP00000513149.1:n.956-15649G>T
ENST00000697161.1:c.591G>T	ENSP00000513150.1:n.591G>T
ENST00000697162.1:c.984G>T	ENSP00000513151.1:n.984G>T
ENST00000697163.1:c.1055G>T	ENSP00000513152.1:p.Gly352Val
ENST00000697164.1:c.965G>T	ENSP00000513153.1:p.Gly322Val
ENST00000697165.1:c.752G>T	ENSP00000513154.1:p.Gly251Val
ENST00000697223.1:c.804G>T	ENSP00000513190.1:n.804G>T
ENST00000697224.1:c.884+3386G>T	ENSP00000513191.1:n.884+3386G>T
ENST00000697225.1:c.658G>T	ENSP00000513192.1:n.658G>T
ENST00000697226.1:c.738+3386G>T	ENSP00000513193.1:n.738+3386G>T
ENST00000697227.1:c.891G>T	ENSP00000513194.1:n.891G>T
ENST00000697228.1:c.747G>T	ENSP00000513195.1:n.747G>T
ENST00000697229.1:c.885-15649G>T	ENSP00000513196.1:n.885-15649G>T
ENST00000697230.1:c.965G>T	ENSP00000513197.1:p.Gly322Val
ENST00000697231.1:c.960G>T	ENSP00000513198.1:n.960G>T
ENST00000697232.1:c.984G>T	ENSP00000513199.1:n.984G>T
ENST00000347310.10:c.1055G>T MANE Select	ENSP00000321345.5:p.Gly352Val
ENST00000637002.1:c.446G>T	ENSP00000490340.1:p.Gly149Val
ENST00000347310.9:c.1055G>T	ENSP00000321345.5:p.Gly352Val
ENST00000395227.2:c.-58-15649G>T	ENSP00000378652.2:n.-58-15649G>T
ENST00000425614.3:c.290G>T	ENSP00000387640.2:p.Gly97Val
ENST00000473881.2:c.191-15649G>T	ENSP00000486667.1:n.191-15649G>T
NM_144701.2:c.1055G>T	NP_653302.2:p.Gly352Val
XM_005270516.2:c.293G>T	XP_005270573.1:p.Gly98Val
XM_011540789.1:c.1145G>T	XP_011539091.1:p.Gly382Val
XM_011540790.1:c.1055G>T	XP_011539092.1:p.Gly352Val
XM_011540791.1:c.1055G>T	XP_011539093.1:p.Gly352Val
XM_011540790.3:c.1055G>T	XP_011539092.1:p.Gly352Val
XM_011540791.3:c.1055G>T	XP_011539093.1:p.Gly352Val
XR_001736993.1:n.1228+3386G>T
NM_144701.3:c.1055G>T MANE Select	NP_653302.2:p.Gly352Val