Canonical Allele Identifier: CA340729743

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724738C>A (hg19) ; chr1:g.67259055C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259055C>A , CM000663.2:g.67259055C>A	GRCh38
NC_000001.10:g.67724738C>A , CM000663.1:g.67724738C>A	GRCh37
NC_000001.9:g.67497326C>A	NCBI36
NG_011498.1:g.97570C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1656C>A	ENSP00000513138.1:n.1656C>A
ENST00000697150.1:c.1714C>A	ENSP00000513139.1:n.1714C>A
ENST00000697151.1:c.1647C>A	ENSP00000513140.1:n.1647C>A
ENST00000697164.1:c.1727C>A	ENSP00000513153.1:p.Pro576Gln
ENST00000697165.1:c.1514C>A	ENSP00000513154.1:p.Pro505Gln
ENST00000347310.10:c.1817C>A MANE Select	ENSP00000321345.5:p.Pro606Gln
ENST00000637002.1:c.1208C>A	ENSP00000490340.1:p.Pro403Gln
ENST00000347310.9:c.1817C>A	ENSP00000321345.5:p.Pro606Gln
ENST00000395227.2:c.611C>A	ENSP00000378652.2:p.Pro204Gln
ENST00000425614.3:c.1052C>A	ENSP00000387640.2:p.Pro351Gln
ENST00000473881.2:c.*643C>A	ENSP00000486667.1:n.*643C>A
NM_144701.2:c.1817C>A	NP_653302.2:p.Pro606Gln
XM_005270516.2:c.1055C>A	XP_005270573.1:p.Pro352Gln
XM_011540789.1:c.1907C>A	XP_011539091.1:p.Pro636Gln
XM_011540790.1:c.1817C>A	XP_011539092.1:p.Pro606Gln
XM_011540791.1:c.1817C>A	XP_011539093.1:p.Pro606Gln
XM_011540790.3:c.1817C>A	XP_011539092.1:p.Pro606Gln
XM_011540791.3:c.1817C>A	XP_011539093.1:p.Pro606Gln
XR_001736993.1:n.1897C>A
NM_144701.3:c.1817C>A MANE Select	NP_653302.2:p.Pro606Gln