Canonical Allele Identifier: CA340729255

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724611C>T (hg19) ; chr1:g.67258928C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258928C>T , CM000663.2:g.67258928C>T	GRCh38
NC_000001.10:g.67724611C>T , CM000663.1:g.67724611C>T	GRCh37
NC_000001.9:g.67497199C>T	NCBI36
NG_011498.1:g.97443C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1529C>T	ENSP00000513138.1:n.1529C>T
ENST00000697150.1:c.1587C>T	ENSP00000513139.1:n.1587C>T
ENST00000697151.1:c.1520C>T	ENSP00000513140.1:n.1520C>T
ENST00000697164.1:c.1600C>T	ENSP00000513153.1:p.Gln534Ter
ENST00000697165.1:c.1387C>T	ENSP00000513154.1:p.Gln463Ter
ENST00000347310.10:c.1690C>T MANE Select	ENSP00000321345.5:p.Gln564Ter
ENST00000637002.1:c.1081C>T	ENSP00000490340.1:p.Gln361Ter
ENST00000347310.9:c.1690C>T	ENSP00000321345.5:p.Gln564Ter
ENST00000395227.2:c.484C>T	ENSP00000378652.2:p.Gln162Ter
ENST00000425614.3:c.925C>T	ENSP00000387640.2:p.Gln309Ter
ENST00000473881.2:c.*516C>T	ENSP00000486667.1:n.*516C>T
NM_144701.2:c.1690C>T	NP_653302.2:p.Gln564Ter
XM_005270516.2:c.928C>T	XP_005270573.1:p.Gln310Ter
XM_011540789.1:c.1780C>T	XP_011539091.1:p.Gln594Ter
XM_011540790.1:c.1690C>T	XP_011539092.1:p.Gln564Ter
XM_011540791.1:c.1690C>T	XP_011539093.1:p.Gln564Ter
XM_011540790.3:c.1690C>T	XP_011539092.1:p.Gln564Ter
XM_011540791.3:c.1690C>T	XP_011539093.1:p.Gln564Ter
XR_001736993.1:n.1770C>T
NM_144701.3:c.1690C>T MANE Select	NP_653302.2:p.Gln564Ter