Canonical Allele Identifier: CA418438739

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724706C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259023C>A , CM000663.2:g.67259023C>A	GRCh38
NC_000001.10:g.67724706C>A , CM000663.1:g.67724706C>A	GRCh37
NC_000001.9:g.67497294C>A	NCBI36
NG_011498.1:g.97538C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1624C>A	ENSP00000513138.1:n.1624C>A
ENST00000697150.1:c.1682C>A	ENSP00000513139.1:n.1682C>A
ENST00000697151.1:c.1615C>A	ENSP00000513140.1:n.1615C>A
ENST00000697164.1:c.1695C>A	ENSP00000513153.1:p.Val565=
ENST00000697165.1:c.1482C>A	ENSP00000513154.1:p.Val494=
ENST00000347310.10:c.1785C>A MANE Select	ENSP00000321345.5:p.Val595=
ENST00000637002.1:c.1176C>A	ENSP00000490340.1:p.Val392=
ENST00000347310.9:c.1785C>A	ENSP00000321345.5:p.Val595=
ENST00000395227.2:c.579C>A	ENSP00000378652.2:p.Val193=
ENST00000425614.3:c.1020C>A	ENSP00000387640.2:p.Val340=
ENST00000473881.2:c.*611C>A	ENSP00000486667.1:n.*611C>A
NM_144701.2:c.1785C>A	NP_653302.2:p.Val595=
XM_005270516.2:c.1023C>A	XP_005270573.1:p.Val341=
XM_011540789.1:c.1875C>A	XP_011539091.1:p.Val625=
XM_011540790.1:c.1785C>A	XP_011539092.1:p.Val595=
XM_011540791.1:c.1785C>A	XP_011539093.1:p.Val595=
XM_011540790.3:c.1785C>A	XP_011539092.1:p.Val595=
XM_011540791.3:c.1785C>A	XP_011539093.1:p.Val595=
XR_001736993.1:n.1865C>A
NM_144701.3:c.1785C>A MANE Select	NP_653302.2:p.Val595=