Canonical Allele Identifier: CA340728750

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724495A>G (hg19) ; chr1:g.67258812A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258812A>G , CM000663.2:g.67258812A>G	GRCh38
NC_000001.10:g.67724495A>G , CM000663.1:g.67724495A>G	GRCh37
NC_000001.9:g.67497083A>G	NCBI36
NG_011498.1:g.97327A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1413A>G	ENSP00000513138.1:n.1413A>G
ENST00000697150.1:c.1471A>G	ENSP00000513139.1:n.1471A>G
ENST00000697151.1:c.1404A>G	ENSP00000513140.1:n.1404A>G
ENST00000697164.1:c.1484A>G	ENSP00000513153.1:p.Gln495Arg
ENST00000697165.1:c.1271A>G	ENSP00000513154.1:p.Gln424Arg
ENST00000347310.10:c.1574A>G MANE Select	ENSP00000321345.5:p.Gln525Arg
ENST00000637002.1:c.965A>G	ENSP00000490340.1:p.Gln322Arg
ENST00000347310.9:c.1574A>G	ENSP00000321345.5:p.Gln525Arg
ENST00000395227.2:c.368A>G	ENSP00000378652.2:p.Gln123Arg
ENST00000425614.3:c.809A>G	ENSP00000387640.2:p.Gln270Arg
ENST00000473881.2:c.*400A>G	ENSP00000486667.1:n.*400A>G
NM_144701.2:c.1574A>G	NP_653302.2:p.Gln525Arg
XM_005270516.2:c.812A>G	XP_005270573.1:p.Gln271Arg
XM_011540789.1:c.1664A>G	XP_011539091.1:p.Gln555Arg
XM_011540790.1:c.1574A>G	XP_011539092.1:p.Gln525Arg
XM_011540791.1:c.1574A>G	XP_011539093.1:p.Gln525Arg
XM_011540790.3:c.1574A>G	XP_011539092.1:p.Gln525Arg
XM_011540791.3:c.1574A>G	XP_011539093.1:p.Gln525Arg
XR_001736993.1:n.1654A>G
NM_144701.3:c.1574A>G MANE Select	NP_653302.2:p.Gln525Arg