Canonical Allele Identifier: CA340728616

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724432T>C (hg19) ; chr1:g.67258749T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258749T>C , CM000663.2:g.67258749T>C	GRCh38
NC_000001.10:g.67724432T>C , CM000663.1:g.67724432T>C	GRCh37
NC_000001.9:g.67497020T>C	NCBI36
NG_011498.1:g.97264T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1350T>C	ENSP00000513138.1:n.1350T>C
ENST00000697150.1:c.1408T>C	ENSP00000513139.1:n.1408T>C
ENST00000697151.1:c.1341T>C	ENSP00000513140.1:n.1341T>C
ENST00000697164.1:c.1421T>C	ENSP00000513153.1:p.Ile474Thr
ENST00000697165.1:c.1208T>C	ENSP00000513154.1:p.Ile403Thr
ENST00000347310.10:c.1511T>C MANE Select	ENSP00000321345.5:p.Ile504Thr
ENST00000637002.1:c.902T>C	ENSP00000490340.1:p.Ile301Thr
ENST00000347310.9:c.1511T>C	ENSP00000321345.5:p.Ile504Thr
ENST00000395227.2:c.305T>C	ENSP00000378652.2:p.Ile102Thr
ENST00000425614.3:c.746T>C	ENSP00000387640.2:p.Ile249Thr
ENST00000473881.2:c.*337T>C	ENSP00000486667.1:n.*337T>C
NM_144701.2:c.1511T>C	NP_653302.2:p.Ile504Thr
XM_005270516.2:c.749T>C	XP_005270573.1:p.Ile250Thr
XM_011540789.1:c.1601T>C	XP_011539091.1:p.Ile534Thr
XM_011540790.1:c.1511T>C	XP_011539092.1:p.Ile504Thr
XM_011540791.1:c.1511T>C	XP_011539093.1:p.Ile504Thr
XM_011540790.3:c.1511T>C	XP_011539092.1:p.Ile504Thr
XM_011540791.3:c.1511T>C	XP_011539093.1:p.Ile504Thr
XR_001736993.1:n.1591T>C
NM_144701.3:c.1511T>C MANE Select	NP_653302.2:p.Ile504Thr