Canonical Allele Identifier: CA418438701

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724676A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258993A>C , CM000663.2:g.67258993A>C	GRCh38
NC_000001.10:g.67724676A>C , CM000663.1:g.67724676A>C	GRCh37
NC_000001.9:g.67497264A>C	NCBI36
NG_011498.1:g.97508A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1594A>C	ENSP00000513138.1:n.1594A>C
ENST00000697150.1:c.1652A>C	ENSP00000513139.1:n.1652A>C
ENST00000697151.1:c.1585A>C	ENSP00000513140.1:n.1585A>C
ENST00000697164.1:c.1665A>C	ENSP00000513153.1:p.Pro555=
ENST00000697165.1:c.1452A>C	ENSP00000513154.1:p.Pro484=
ENST00000347310.10:c.1755A>C MANE Select	ENSP00000321345.5:p.Pro585=
ENST00000637002.1:c.1146A>C	ENSP00000490340.1:p.Pro382=
ENST00000347310.9:c.1755A>C	ENSP00000321345.5:p.Pro585=
ENST00000395227.2:c.549A>C	ENSP00000378652.2:p.Pro183=
ENST00000425614.3:c.990A>C	ENSP00000387640.2:p.Pro330=
ENST00000473881.2:c.*581A>C	ENSP00000486667.1:n.*581A>C
NM_144701.2:c.1755A>C	NP_653302.2:p.Pro585=
XM_005270516.2:c.993A>C	XP_005270573.1:p.Pro331=
XM_011540789.1:c.1845A>C	XP_011539091.1:p.Pro615=
XM_011540790.1:c.1755A>C	XP_011539092.1:p.Pro585=
XM_011540791.1:c.1755A>C	XP_011539093.1:p.Pro585=
XM_011540790.3:c.1755A>C	XP_011539092.1:p.Pro585=
XM_011540791.3:c.1755A>C	XP_011539093.1:p.Pro585=
XR_001736993.1:n.1835A>C
NM_144701.3:c.1755A>C MANE Select	NP_653302.2:p.Pro585=