Canonical Allele Identifier: CA899932

Gene: IL23R

Linked Data

• dbSNP Id: rs375552098
• ExAC: 1:67705894 A / G
• gnomAD v2: 1-67705894-A-G
• gnomAD v3: 1-67240211-A-G
• gnomAD v4: 1-67240211-A-G
• MyVariant Identifiers: chr1:g.67705894A>G (hg19) ; chr1:g.67240211A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67240211A>G , CM000663.2:g.67240211A>G	GRCh38
NC_000001.10:g.67705894A>G , CM000663.1:g.67705894A>G	GRCh37
NC_000001.9:g.67478482A>G	NCBI36
NG_011498.1:g.78726A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000697148.1:c.954A>G	ENSP00000513137.1:n.954A>G
ENST00000697149.1:c.917A>G	ENSP00000513138.1:n.917A>G
ENST00000697150.1:c.1045+3409A>G	ENSP00000513139.1:n.1045+3409A>G
ENST00000697151.1:c.1045+3409A>G	ENSP00000513140.1:n.1045+3409A>G
ENST00000697152.1:c.799-15626A>G	ENSP00000513141.1:n.799-15626A>G
ENST00000697153.1:c.795-15626A>G	ENSP00000513142.1:n.795-15626A>G
ENST00000697154.1:c.956-18267A>G	ENSP00000513143.1:n.956-18267A>G
ENST00000697155.1:c.649-18267A>G	ENSP00000513144.1:n.649-18267A>G
ENST00000697156.1:c.1078A>G	ENSP00000513145.1:p.Met360Val
ENST00000697157.1:c.932A>G	ENSP00000513146.1:n.932A>G
ENST00000697158.1:c.921A>G	ENSP00000513147.1:n.921A>G
ENST00000697159.1:c.771A>G	ENSP00000513148.1:n.771A>G
ENST00000697160.1:c.956-15626A>G	ENSP00000513149.1:n.956-15626A>G
ENST00000697161.1:c.614A>G	ENSP00000513150.1:n.614A>G
ENST00000697162.1:c.1007A>G	ENSP00000513151.1:n.1007A>G
ENST00000697163.1:c.1078A>G	ENSP00000513152.1:p.Met360Val
ENST00000697164.1:c.988A>G	ENSP00000513153.1:p.Met330Val
ENST00000697165.1:c.775A>G	ENSP00000513154.1:p.Met259Val
ENST00000697223.1:c.827A>G	ENSP00000513190.1:n.827A>G
ENST00000697224.1:c.884+3409A>G	ENSP00000513191.1:n.884+3409A>G
ENST00000697225.1:c.681A>G	ENSP00000513192.1:n.681A>G
ENST00000697226.1:c.738+3409A>G	ENSP00000513193.1:n.738+3409A>G
ENST00000697227.1:c.914A>G	ENSP00000513194.1:n.914A>G
ENST00000697228.1:c.770A>G	ENSP00000513195.1:n.770A>G
ENST00000697229.1:c.885-15626A>G	ENSP00000513196.1:n.885-15626A>G
ENST00000697230.1:c.988A>G	ENSP00000513197.1:p.Met330Val
ENST00000697231.1:c.983A>G	ENSP00000513198.1:n.983A>G
ENST00000697232.1:c.1007A>G	ENSP00000513199.1:n.1007A>G
ENST00000347310.10:c.1078A>G MANE Select	ENSP00000321345.5:p.Met360Val
ENST00000637002.1:c.469A>G	ENSP00000490340.1:p.Met157Val
ENST00000347310.9:c.1078A>G	ENSP00000321345.5:p.Met360Val
ENST00000395227.2:c.-58-15626A>G	ENSP00000378652.2:n.-58-15626A>G
ENST00000425614.3:c.313A>G	ENSP00000387640.2:p.Met105Val
ENST00000473881.2:c.191-15626A>G	ENSP00000486667.1:n.191-15626A>G
NM_144701.2:c.1078A>G	NP_653302.2:p.Met360Val
XM_005270516.2:c.316A>G	XP_005270573.1:p.Met106Val
XM_011540789.1:c.1168A>G	XP_011539091.1:p.Met390Val
XM_011540790.1:c.1078A>G	XP_011539092.1:p.Met360Val
XM_011540791.1:c.1078A>G	XP_011539093.1:p.Met360Val
XM_011540790.3:c.1078A>G	XP_011539092.1:p.Met360Val
XM_011540791.3:c.1078A>G	XP_011539093.1:p.Met360Val
XR_001736993.1:n.1228+3409A>G
NM_144701.3:c.1078A>G MANE Select	NP_653302.2:p.Met360Val