Canonical Allele Identifier: CA340730112

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724795C>A (hg19) ; chr1:g.67259112C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259112C>A , CM000663.2:g.67259112C>A	GRCh38
NC_000001.10:g.67724795C>A , CM000663.1:g.67724795C>A	GRCh37
NC_000001.9:g.67497383C>A	NCBI36
NG_011498.1:g.97627C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000697149.1:c.1713C>A	ENSP00000513138.1:n.1713C>A
ENST00000697150.1:c.1771C>A	ENSP00000513139.1:n.1771C>A
ENST00000697151.1:c.1704C>A	ENSP00000513140.1:n.1704C>A
ENST00000697164.1:c.1784C>A	ENSP00000513153.1:p.Ser595Ter
ENST00000697165.1:c.1571C>A	ENSP00000513154.1:p.Ser524Ter
ENST00000347310.10:c.1874C>A MANE Select	ENSP00000321345.5:p.Ser625Ter
ENST00000637002.1:c.1265C>A	ENSP00000490340.1:p.Ser422Ter
ENST00000347310.9:c.1874C>A	ENSP00000321345.5:p.Ser625Ter
ENST00000395227.2:c.668C>A	ENSP00000378652.2:p.Ser223Ter
ENST00000425614.3:c.1109C>A	ENSP00000387640.2:p.Ser370Ter
ENST00000473881.2:c.*700C>A	ENSP00000486667.1:n.*700C>A
NM_144701.2:c.1874C>A	NP_653302.2:p.Ser625Ter
XM_005270516.2:c.1112C>A	XP_005270573.1:p.Ser371Ter
XM_011540789.1:c.1964C>A	XP_011539091.1:p.Ser655Ter
XM_011540790.1:c.1874C>A	XP_011539092.1:p.Ser625Ter
XM_011540791.1:c.1874C>A	XP_011539093.1:p.Ser625Ter
XM_011540790.3:c.1874C>A	XP_011539092.1:p.Ser625Ter
XM_011540791.3:c.1874C>A	XP_011539093.1:p.Ser625Ter
XR_001736993.1:n.1954C>A
NM_144701.3:c.1874C>A MANE Select	NP_653302.2:p.Ser625Ter