Canonical Allele Identifier: CA418438754

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724514T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258831T>C , CM000663.2:g.67258831T>C	GRCh38
NC_000001.10:g.67724514T>C , CM000663.1:g.67724514T>C	GRCh37
NC_000001.9:g.67497102T>C	NCBI36
NG_011498.1:g.97346T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1432T>C	ENSP00000513138.1:n.1432T>C
ENST00000697150.1:c.1490T>C	ENSP00000513139.1:n.1490T>C
ENST00000697151.1:c.1423T>C	ENSP00000513140.1:n.1423T>C
ENST00000697164.1:c.1503T>C	ENSP00000513153.1:p.Ala501=
ENST00000697165.1:c.1290T>C	ENSP00000513154.1:p.Ala430=
ENST00000347310.10:c.1593T>C MANE Select	ENSP00000321345.5:p.Ala531=
ENST00000637002.1:c.984T>C	ENSP00000490340.1:p.Ala328=
ENST00000347310.9:c.1593T>C	ENSP00000321345.5:p.Ala531=
ENST00000395227.2:c.387T>C	ENSP00000378652.2:p.Ala129=
ENST00000425614.3:c.828T>C	ENSP00000387640.2:p.Ala276=
ENST00000473881.2:c.*419T>C	ENSP00000486667.1:n.*419T>C
NM_144701.2:c.1593T>C	NP_653302.2:p.Ala531=
XM_005270516.2:c.831T>C	XP_005270573.1:p.Ala277=
XM_011540789.1:c.1683T>C	XP_011539091.1:p.Ala561=
XM_011540790.1:c.1593T>C	XP_011539092.1:p.Ala531=
XM_011540791.1:c.1593T>C	XP_011539093.1:p.Ala531=
XM_011540790.3:c.1593T>C	XP_011539092.1:p.Ala531=
XM_011540791.3:c.1593T>C	XP_011539093.1:p.Ala531=
XR_001736993.1:n.1673T>C
NM_144701.3:c.1593T>C MANE Select	NP_653302.2:p.Ala531=