Canonical Allele Identifier: CA418438717

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724484T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258801T>C , CM000663.2:g.67258801T>C	GRCh38
NC_000001.10:g.67724484T>C , CM000663.1:g.67724484T>C	GRCh37
NC_000001.9:g.67497072T>C	NCBI36
NG_011498.1:g.97316T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1402T>C	ENSP00000513138.1:n.1402T>C
ENST00000697150.1:c.1460T>C	ENSP00000513139.1:n.1460T>C
ENST00000697151.1:c.1393T>C	ENSP00000513140.1:n.1393T>C
ENST00000697164.1:c.1473T>C	ENSP00000513153.1:p.Asn491=
ENST00000697165.1:c.1260T>C	ENSP00000513154.1:p.Asn420=
ENST00000347310.10:c.1563T>C MANE Select	ENSP00000321345.5:p.Asn521=
ENST00000637002.1:c.954T>C	ENSP00000490340.1:p.Asn318=
ENST00000347310.9:c.1563T>C	ENSP00000321345.5:p.Asn521=
ENST00000395227.2:c.357T>C	ENSP00000378652.2:p.Asn119=
ENST00000425614.3:c.798T>C	ENSP00000387640.2:p.Asn266=
ENST00000473881.2:c.*389T>C	ENSP00000486667.1:n.*389T>C
NM_144701.2:c.1563T>C	NP_653302.2:p.Asn521=
XM_005270516.2:c.801T>C	XP_005270573.1:p.Asn267=
XM_011540789.1:c.1653T>C	XP_011539091.1:p.Asn551=
XM_011540790.1:c.1563T>C	XP_011539092.1:p.Asn521=
XM_011540791.1:c.1563T>C	XP_011539093.1:p.Asn521=
XM_011540790.3:c.1563T>C	XP_011539092.1:p.Asn521=
XM_011540791.3:c.1563T>C	XP_011539093.1:p.Asn521=
XR_001736993.1:n.1643T>C
NM_144701.3:c.1563T>C MANE Select	NP_653302.2:p.Asn521=