Canonical Allele Identifier: CA418438779

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724538A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258855A>C , CM000663.2:g.67258855A>C	GRCh38
NC_000001.10:g.67724538A>C , CM000663.1:g.67724538A>C	GRCh37
NC_000001.9:g.67497126A>C	NCBI36
NG_011498.1:g.97370A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1456A>C	ENSP00000513138.1:n.1456A>C
ENST00000697150.1:c.1514A>C	ENSP00000513139.1:n.1514A>C
ENST00000697151.1:c.1447A>C	ENSP00000513140.1:n.1447A>C
ENST00000697164.1:c.1527A>C	ENSP00000513153.1:p.Ser509=
ENST00000697165.1:c.1314A>C	ENSP00000513154.1:p.Ser438=
ENST00000347310.10:c.1617A>C MANE Select	ENSP00000321345.5:p.Ser539=
ENST00000637002.1:c.1008A>C	ENSP00000490340.1:p.Ser336=
ENST00000347310.9:c.1617A>C	ENSP00000321345.5:p.Ser539=
ENST00000395227.2:c.411A>C	ENSP00000378652.2:p.Ser137=
ENST00000425614.3:c.852A>C	ENSP00000387640.2:p.Ser284=
ENST00000473881.2:c.*443A>C	ENSP00000486667.1:n.*443A>C
NM_144701.2:c.1617A>C	NP_653302.2:p.Ser539=
XM_005270516.2:c.855A>C	XP_005270573.1:p.Ser285=
XM_011540789.1:c.1707A>C	XP_011539091.1:p.Ser569=
XM_011540790.1:c.1617A>C	XP_011539092.1:p.Ser539=
XM_011540791.1:c.1617A>C	XP_011539093.1:p.Ser539=
XM_011540790.3:c.1617A>C	XP_011539092.1:p.Ser539=
XM_011540791.3:c.1617A>C	XP_011539093.1:p.Ser539=
XR_001736993.1:n.1697A>C
NM_144701.3:c.1617A>C MANE Select	NP_653302.2:p.Ser539=