Canonical Allele Identifier: CA340729502

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724672T>C (hg19) ; chr1:g.67258989T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258989T>C , CM000663.2:g.67258989T>C	GRCh38
NC_000001.10:g.67724672T>C , CM000663.1:g.67724672T>C	GRCh37
NC_000001.9:g.67497260T>C	NCBI36
NG_011498.1:g.97504T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1590T>C	ENSP00000513138.1:n.1590T>C
ENST00000697150.1:c.1648T>C	ENSP00000513139.1:n.1648T>C
ENST00000697151.1:c.1581T>C	ENSP00000513140.1:n.1581T>C
ENST00000697164.1:c.1661T>C	ENSP00000513153.1:p.Ile554Thr
ENST00000697165.1:c.1448T>C	ENSP00000513154.1:p.Ile483Thr
ENST00000347310.10:c.1751T>C MANE Select	ENSP00000321345.5:p.Ile584Thr
ENST00000637002.1:c.1142T>C	ENSP00000490340.1:p.Ile381Thr
ENST00000347310.9:c.1751T>C	ENSP00000321345.5:p.Ile584Thr
ENST00000395227.2:c.545T>C	ENSP00000378652.2:p.Ile182Thr
ENST00000425614.3:c.986T>C	ENSP00000387640.2:p.Ile329Thr
ENST00000473881.2:c.*577T>C	ENSP00000486667.1:n.*577T>C
NM_144701.2:c.1751T>C	NP_653302.2:p.Ile584Thr
XM_005270516.2:c.989T>C	XP_005270573.1:p.Ile330Thr
XM_011540789.1:c.1841T>C	XP_011539091.1:p.Ile614Thr
XM_011540790.1:c.1751T>C	XP_011539092.1:p.Ile584Thr
XM_011540791.1:c.1751T>C	XP_011539093.1:p.Ile584Thr
XM_011540790.3:c.1751T>C	XP_011539092.1:p.Ile584Thr
XM_011540791.3:c.1751T>C	XP_011539093.1:p.Ile584Thr
XR_001736993.1:n.1831T>C
NM_144701.3:c.1751T>C MANE Select	NP_653302.2:p.Ile584Thr