Canonical Allele Identifier: CA340729640

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724712T>A (hg19) ; chr1:g.67259029T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259029T>A , CM000663.2:g.67259029T>A	GRCh38
NC_000001.10:g.67724712T>A , CM000663.1:g.67724712T>A	GRCh37
NC_000001.9:g.67497300T>A	NCBI36
NG_011498.1:g.97544T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1630T>A	ENSP00000513138.1:n.1630T>A
ENST00000697150.1:c.1688T>A	ENSP00000513139.1:n.1688T>A
ENST00000697151.1:c.1621T>A	ENSP00000513140.1:n.1621T>A
ENST00000697164.1:c.1701T>A	ENSP00000513153.1:p.Cys567Ter
ENST00000697165.1:c.1488T>A	ENSP00000513154.1:p.Cys496Ter
ENST00000347310.10:c.1791T>A MANE Select	ENSP00000321345.5:p.Cys597Ter
ENST00000637002.1:c.1182T>A	ENSP00000490340.1:p.Cys394Ter
ENST00000347310.9:c.1791T>A	ENSP00000321345.5:p.Cys597Ter
ENST00000395227.2:c.585T>A	ENSP00000378652.2:p.Cys195Ter
ENST00000425614.3:c.1026T>A	ENSP00000387640.2:p.Cys342Ter
ENST00000473881.2:c.*617T>A	ENSP00000486667.1:n.*617T>A
NM_144701.2:c.1791T>A	NP_653302.2:p.Cys597Ter
XM_005270516.2:c.1029T>A	XP_005270573.1:p.Cys343Ter
XM_011540789.1:c.1881T>A	XP_011539091.1:p.Cys627Ter
XM_011540790.1:c.1791T>A	XP_011539092.1:p.Cys597Ter
XM_011540791.1:c.1791T>A	XP_011539093.1:p.Cys597Ter
XM_011540790.3:c.1791T>A	XP_011539092.1:p.Cys597Ter
XM_011540791.3:c.1791T>A	XP_011539093.1:p.Cys597Ter
XR_001736993.1:n.1871T>A
NM_144701.3:c.1791T>A MANE Select	NP_653302.2:p.Cys597Ter