Canonical Allele Identifier: CA418438708

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724478A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258795A>C , CM000663.2:g.67258795A>C	GRCh38
NC_000001.10:g.67724478A>C , CM000663.1:g.67724478A>C	GRCh37
NC_000001.9:g.67497066A>C	NCBI36
NG_011498.1:g.97310A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1396A>C	ENSP00000513138.1:n.1396A>C
ENST00000697150.1:c.1454A>C	ENSP00000513139.1:n.1454A>C
ENST00000697151.1:c.1387A>C	ENSP00000513140.1:n.1387A>C
ENST00000697164.1:c.1467A>C	ENSP00000513153.1:p.Gly489=
ENST00000697165.1:c.1254A>C	ENSP00000513154.1:p.Gly418=
ENST00000347310.10:c.1557A>C MANE Select	ENSP00000321345.5:p.Gly519=
ENST00000637002.1:c.948A>C	ENSP00000490340.1:p.Gly316=
ENST00000347310.9:c.1557A>C	ENSP00000321345.5:p.Gly519=
ENST00000395227.2:c.351A>C	ENSP00000378652.2:p.Gly117=
ENST00000425614.3:c.792A>C	ENSP00000387640.2:p.Gly264=
ENST00000473881.2:c.*383A>C	ENSP00000486667.1:n.*383A>C
NM_144701.2:c.1557A>C	NP_653302.2:p.Gly519=
XM_005270516.2:c.795A>C	XP_005270573.1:p.Gly265=
XM_011540789.1:c.1647A>C	XP_011539091.1:p.Gly549=
XM_011540790.1:c.1557A>C	XP_011539092.1:p.Gly519=
XM_011540791.1:c.1557A>C	XP_011539093.1:p.Gly519=
XM_011540790.3:c.1557A>C	XP_011539092.1:p.Gly519=
XM_011540791.3:c.1557A>C	XP_011539093.1:p.Gly519=
XR_001736993.1:n.1637A>C
NM_144701.3:c.1557A>C MANE Select	NP_653302.2:p.Gly519=