Canonical Allele Identifier: CA340729999

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724782T>G (hg19) ; chr1:g.67259099T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259099T>G , CM000663.2:g.67259099T>G	GRCh38
NC_000001.10:g.67724782T>G , CM000663.1:g.67724782T>G	GRCh37
NC_000001.9:g.67497370T>G	NCBI36
NG_011498.1:g.97614T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1700T>G	ENSP00000513138.1:n.1700T>G
ENST00000697150.1:c.1758T>G	ENSP00000513139.1:n.1758T>G
ENST00000697151.1:c.1691T>G	ENSP00000513140.1:n.1691T>G
ENST00000697164.1:c.1771T>G	ENSP00000513153.1:p.Phe591Val
ENST00000697165.1:c.1558T>G	ENSP00000513154.1:p.Phe520Val
ENST00000347310.10:c.1861T>G MANE Select	ENSP00000321345.5:p.Phe621Val
ENST00000637002.1:c.1252T>G	ENSP00000490340.1:p.Phe418Val
ENST00000347310.9:c.1861T>G	ENSP00000321345.5:p.Phe621Val
ENST00000395227.2:c.655T>G	ENSP00000378652.2:p.Phe219Val
ENST00000425614.3:c.1096T>G	ENSP00000387640.2:p.Phe366Val
ENST00000473881.2:c.*687T>G	ENSP00000486667.1:n.*687T>G
NM_144701.2:c.1861T>G	NP_653302.2:p.Phe621Val
XM_005270516.2:c.1099T>G	XP_005270573.1:p.Phe367Val
XM_011540789.1:c.1951T>G	XP_011539091.1:p.Phe651Val
XM_011540790.1:c.1861T>G	XP_011539092.1:p.Phe621Val
XM_011540791.1:c.1861T>G	XP_011539093.1:p.Phe621Val
XM_011540790.3:c.1861T>G	XP_011539092.1:p.Phe621Val
XM_011540791.3:c.1861T>G	XP_011539093.1:p.Phe621Val
XR_001736993.1:n.1941T>G
NM_144701.3:c.1861T>G MANE Select	NP_653302.2:p.Phe621Val