Canonical Allele Identifier: CA340729477

Gene: IL23R

Linked Data

• dbSNP Id: rs1295997830
• gnomAD v2: 1-67724666-A-G
• MyVariant Identifiers: chr1:g.67724666A>G (hg19) ; chr1:g.67258983A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258983A>G , CM000663.2:g.67258983A>G	GRCh38
NC_000001.10:g.67724666A>G , CM000663.1:g.67724666A>G	GRCh37
NC_000001.9:g.67497254A>G	NCBI36
NG_011498.1:g.97498A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1584A>G	ENSP00000513138.1:n.1584A>G
ENST00000697150.1:c.1642A>G	ENSP00000513139.1:n.1642A>G
ENST00000697151.1:c.1575A>G	ENSP00000513140.1:n.1575A>G
ENST00000697164.1:c.1655A>G	ENSP00000513153.1:p.Glu552Gly
ENST00000697165.1:c.1442A>G	ENSP00000513154.1:p.Glu481Gly
ENST00000347310.10:c.1745A>G MANE Select	ENSP00000321345.5:p.Glu582Gly
ENST00000637002.1:c.1136A>G	ENSP00000490340.1:p.Glu379Gly
ENST00000347310.9:c.1745A>G	ENSP00000321345.5:p.Glu582Gly
ENST00000395227.2:c.539A>G	ENSP00000378652.2:p.Glu180Gly
ENST00000425614.3:c.980A>G	ENSP00000387640.2:p.Glu327Gly
ENST00000473881.2:c.*571A>G	ENSP00000486667.1:n.*571A>G
NM_144701.2:c.1745A>G	NP_653302.2:p.Glu582Gly
XM_005270516.2:c.983A>G	XP_005270573.1:p.Glu328Gly
XM_011540789.1:c.1835A>G	XP_011539091.1:p.Glu612Gly
XM_011540790.1:c.1745A>G	XP_011539092.1:p.Glu582Gly
XM_011540791.1:c.1745A>G	XP_011539093.1:p.Glu582Gly
XM_011540790.3:c.1745A>G	XP_011539092.1:p.Glu582Gly
XM_011540791.3:c.1745A>G	XP_011539093.1:p.Glu582Gly
XR_001736993.1:n.1825A>G
NM_144701.3:c.1745A>G MANE Select	NP_653302.2:p.Glu582Gly