Canonical Allele Identifier: CA418438824

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724784C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259101C>T , CM000663.2:g.67259101C>T	GRCh38
NC_000001.10:g.67724784C>T , CM000663.1:g.67724784C>T	GRCh37
NC_000001.9:g.67497372C>T	NCBI36
NG_011498.1:g.97616C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1702C>T	ENSP00000513138.1:n.1702C>T
ENST00000697150.1:c.1760C>T	ENSP00000513139.1:n.1760C>T
ENST00000697151.1:c.1693C>T	ENSP00000513140.1:n.1693C>T
ENST00000697164.1:c.1773C>T	ENSP00000513153.1:p.Phe591=
ENST00000697165.1:c.1560C>T	ENSP00000513154.1:p.Phe520=
ENST00000347310.10:c.1863C>T MANE Select	ENSP00000321345.5:p.Phe621=
ENST00000637002.1:c.1254C>T	ENSP00000490340.1:p.Phe418=
ENST00000347310.9:c.1863C>T	ENSP00000321345.5:p.Phe621=
ENST00000395227.2:c.657C>T	ENSP00000378652.2:p.Phe219=
ENST00000425614.3:c.1098C>T	ENSP00000387640.2:p.Phe366=
ENST00000473881.2:c.*689C>T	ENSP00000486667.1:n.*689C>T
NM_144701.2:c.1863C>T	NP_653302.2:p.Phe621=
XM_005270516.2:c.1101C>T	XP_005270573.1:p.Phe367=
XM_011540789.1:c.1953C>T	XP_011539091.1:p.Phe651=
XM_011540790.1:c.1863C>T	XP_011539092.1:p.Phe621=
XM_011540791.1:c.1863C>T	XP_011539093.1:p.Phe621=
XM_011540790.3:c.1863C>T	XP_011539092.1:p.Phe621=
XM_011540791.3:c.1863C>T	XP_011539093.1:p.Phe621=
XR_001736993.1:n.1943C>T
NM_144701.3:c.1863C>T MANE Select	NP_653302.2:p.Phe621=