Canonical Allele Identifier: CA418438737

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724703T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259020T>C , CM000663.2:g.67259020T>C	GRCh38
NC_000001.10:g.67724703T>C , CM000663.1:g.67724703T>C	GRCh37
NC_000001.9:g.67497291T>C	NCBI36
NG_011498.1:g.97535T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1621T>C	ENSP00000513138.1:n.1621T>C
ENST00000697150.1:c.1679T>C	ENSP00000513139.1:n.1679T>C
ENST00000697151.1:c.1612T>C	ENSP00000513140.1:n.1612T>C
ENST00000697164.1:c.1692T>C	ENSP00000513153.1:p.Phe564=
ENST00000697165.1:c.1479T>C	ENSP00000513154.1:p.Phe493=
ENST00000347310.10:c.1782T>C MANE Select	ENSP00000321345.5:p.Phe594=
ENST00000637002.1:c.1173T>C	ENSP00000490340.1:p.Phe391=
ENST00000347310.9:c.1782T>C	ENSP00000321345.5:p.Phe594=
ENST00000395227.2:c.576T>C	ENSP00000378652.2:p.Phe192=
ENST00000425614.3:c.1017T>C	ENSP00000387640.2:p.Phe339=
ENST00000473881.2:c.*608T>C	ENSP00000486667.1:n.*608T>C
NM_144701.2:c.1782T>C	NP_653302.2:p.Phe594=
XM_005270516.2:c.1020T>C	XP_005270573.1:p.Phe340=
XM_011540789.1:c.1872T>C	XP_011539091.1:p.Phe624=
XM_011540790.1:c.1782T>C	XP_011539092.1:p.Phe594=
XM_011540791.1:c.1782T>C	XP_011539093.1:p.Phe594=
XM_011540790.3:c.1782T>C	XP_011539092.1:p.Phe594=
XM_011540791.3:c.1782T>C	XP_011539093.1:p.Phe594=
XR_001736993.1:n.1862T>C
NM_144701.3:c.1782T>C MANE Select	NP_653302.2:p.Phe594=