Canonical Allele Identifier: CA340728575

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724422A>T (hg19) ; chr1:g.67258739A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258739A>T , CM000663.2:g.67258739A>T	GRCh38
NC_000001.10:g.67724422A>T , CM000663.1:g.67724422A>T	GRCh37
NC_000001.9:g.67497010A>T	NCBI36
NG_011498.1:g.97254A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1340A>T	ENSP00000513138.1:n.1340A>T
ENST00000697150.1:c.1398A>T	ENSP00000513139.1:n.1398A>T
ENST00000697151.1:c.1331A>T	ENSP00000513140.1:n.1331A>T
ENST00000697164.1:c.1411A>T	ENSP00000513153.1:p.Asn471Tyr
ENST00000697165.1:c.1198A>T	ENSP00000513154.1:p.Asn400Tyr
ENST00000347310.10:c.1501A>T MANE Select	ENSP00000321345.5:p.Asn501Tyr
ENST00000637002.1:c.892A>T	ENSP00000490340.1:p.Asn298Tyr
ENST00000347310.9:c.1501A>T	ENSP00000321345.5:p.Asn501Tyr
ENST00000395227.2:c.295A>T	ENSP00000378652.2:p.Asn99Tyr
ENST00000425614.3:c.736A>T	ENSP00000387640.2:p.Asn246Tyr
ENST00000473881.2:c.*327A>T	ENSP00000486667.1:n.*327A>T
NM_144701.2:c.1501A>T	NP_653302.2:p.Asn501Tyr
XM_005270516.2:c.739A>T	XP_005270573.1:p.Asn247Tyr
XM_011540789.1:c.1591A>T	XP_011539091.1:p.Asn531Tyr
XM_011540790.1:c.1501A>T	XP_011539092.1:p.Asn501Tyr
XM_011540791.1:c.1501A>T	XP_011539093.1:p.Asn501Tyr
XM_011540790.3:c.1501A>T	XP_011539092.1:p.Asn501Tyr
XM_011540791.3:c.1501A>T	XP_011539093.1:p.Asn501Tyr
XR_001736993.1:n.1581A>T
NM_144701.3:c.1501A>T MANE Select	NP_653302.2:p.Asn501Tyr