Canonical Allele Identifier: CA418438763

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724724G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259041G>C , CM000663.2:g.67259041G>C	GRCh38
NC_000001.10:g.67724724G>C , CM000663.1:g.67724724G>C	GRCh37
NC_000001.9:g.67497312G>C	NCBI36
NG_011498.1:g.97556G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1642G>C	ENSP00000513138.1:n.1642G>C
ENST00000697150.1:c.1700G>C	ENSP00000513139.1:n.1700G>C
ENST00000697151.1:c.1633G>C	ENSP00000513140.1:n.1633G>C
ENST00000697164.1:c.1713G>C	ENSP00000513153.1:p.Val571=
ENST00000697165.1:c.1500G>C	ENSP00000513154.1:p.Val500=
ENST00000347310.10:c.1803G>C MANE Select	ENSP00000321345.5:p.Val601=
ENST00000637002.1:c.1194G>C	ENSP00000490340.1:p.Val398=
ENST00000347310.9:c.1803G>C	ENSP00000321345.5:p.Val601=
ENST00000395227.2:c.597G>C	ENSP00000378652.2:p.Val199=
ENST00000425614.3:c.1038G>C	ENSP00000387640.2:p.Val346=
ENST00000473881.2:c.*629G>C	ENSP00000486667.1:n.*629G>C
NM_144701.2:c.1803G>C	NP_653302.2:p.Val601=
XM_005270516.2:c.1041G>C	XP_005270573.1:p.Val347=
XM_011540789.1:c.1893G>C	XP_011539091.1:p.Val631=
XM_011540790.1:c.1803G>C	XP_011539092.1:p.Val601=
XM_011540791.1:c.1803G>C	XP_011539093.1:p.Val601=
XM_011540790.3:c.1803G>C	XP_011539092.1:p.Val601=
XM_011540791.3:c.1803G>C	XP_011539093.1:p.Val601=
XR_001736993.1:n.1883G>C
NM_144701.3:c.1803G>C MANE Select	NP_653302.2:p.Val601=