Canonical Allele Identifier: CA340730186

Gene: IL23R

Linked Data

• ClinVar Variation Id: 1981876
• ClinVar RCV Id: RCV002766477
• MyVariant Identifiers: chr1:g.67724806A>G (hg19) ; chr1:g.67259123A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259123A>G , CM000663.2:g.67259123A>G	GRCh38
NC_000001.10:g.67724806A>G , CM000663.1:g.67724806A>G	GRCh37
NC_000001.9:g.67497394A>G	NCBI36
NG_011498.1:g.97638A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000697149.1:c.1724A>G	ENSP00000513138.1:n.1724A>G
ENST00000697150.1:c.1782A>G	ENSP00000513139.1:n.1782A>G
ENST00000697151.1:c.1715A>G	ENSP00000513140.1:n.1715A>G
ENST00000697164.1:c.1795A>G	ENSP00000513153.1:p.Lys599Glu
ENST00000697165.1:c.1582A>G	ENSP00000513154.1:p.Lys528Glu
ENST00000347310.10:c.1885A>G MANE Select	ENSP00000321345.5:p.Lys629Glu
ENST00000637002.1:c.1276A>G	ENSP00000490340.1:p.Lys426Glu
ENST00000347310.9:c.1885A>G	ENSP00000321345.5:p.Lys629Glu
ENST00000395227.2:c.679A>G	ENSP00000378652.2:p.Lys227Glu
ENST00000425614.3:c.1120A>G	ENSP00000387640.2:p.Lys374Glu
ENST00000473881.2:c.*711A>G	ENSP00000486667.1:n.*711A>G
NM_144701.2:c.1885A>G	NP_653302.2:p.Lys629Glu
XM_005270516.2:c.1123A>G	XP_005270573.1:p.Lys375Glu
XM_011540789.1:c.1975A>G	XP_011539091.1:p.Lys659Glu
XM_011540790.1:c.1885A>G	XP_011539092.1:p.Lys629Glu
XM_011540791.1:c.1885A>G	XP_011539093.1:p.Lys629Glu
XM_011540790.3:c.1885A>G	XP_011539092.1:p.Lys629Glu
XM_011540791.3:c.1885A>G	XP_011539093.1:p.Lys629Glu
XR_001736993.1:n.1965A>G
NM_144701.3:c.1885A>G MANE Select	NP_653302.2:p.Lys629Glu