Canonical Allele Identifier: CA418438770

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724526A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258843A>T , CM000663.2:g.67258843A>T	GRCh38
NC_000001.10:g.67724526A>T , CM000663.1:g.67724526A>T	GRCh37
NC_000001.9:g.67497114A>T	NCBI36
NG_011498.1:g.97358A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1444A>T	ENSP00000513138.1:n.1444A>T
ENST00000697150.1:c.1502A>T	ENSP00000513139.1:n.1502A>T
ENST00000697151.1:c.1435A>T	ENSP00000513140.1:n.1435A>T
ENST00000697164.1:c.1515A>T	ENSP00000513153.1:p.Ser505=
ENST00000697165.1:c.1302A>T	ENSP00000513154.1:p.Ser434=
ENST00000347310.10:c.1605A>T MANE Select	ENSP00000321345.5:p.Ser535=
ENST00000637002.1:c.996A>T	ENSP00000490340.1:p.Ser332=
ENST00000347310.9:c.1605A>T	ENSP00000321345.5:p.Ser535=
ENST00000395227.2:c.399A>T	ENSP00000378652.2:p.Ser133=
ENST00000425614.3:c.840A>T	ENSP00000387640.2:p.Ser280=
ENST00000473881.2:c.*431A>T	ENSP00000486667.1:n.*431A>T
NM_144701.2:c.1605A>T	NP_653302.2:p.Ser535=
XM_005270516.2:c.843A>T	XP_005270573.1:p.Ser281=
XM_011540789.1:c.1695A>T	XP_011539091.1:p.Ser565=
XM_011540790.1:c.1605A>T	XP_011539092.1:p.Ser535=
XM_011540791.1:c.1605A>T	XP_011539093.1:p.Ser535=
XM_011540790.3:c.1605A>T	XP_011539092.1:p.Ser535=
XM_011540791.3:c.1605A>T	XP_011539093.1:p.Ser535=
XR_001736993.1:n.1685A>T
NM_144701.3:c.1605A>T MANE Select	NP_653302.2:p.Ser535=