Canonical Allele Identifier: CA340730244

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724811G>C (hg19) ; chr1:g.67259128G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259128G>C , CM000663.2:g.67259128G>C	GRCh38
NC_000001.10:g.67724811G>C , CM000663.1:g.67724811G>C	GRCh37
NC_000001.9:g.67497399G>C	NCBI36
NG_011498.1:g.97643G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697164.1:c.1800G>C	ENSP00000513153.1:p.Ter600Tyr
ENST00000697165.1:c.1587G>C	ENSP00000513154.1:p.Ter529Tyr
ENST00000347310.10:c.1890G>C MANE Select	ENSP00000321345.5:p.Ter630Tyr
ENST00000637002.1:c.1281G>C	ENSP00000490340.1:p.Ter427Tyr
ENST00000347310.9:c.1890G>C	ENSP00000321345.5:p.Ter630Tyr
ENST00000395227.2:c.684G>C	ENSP00000378652.2:p.Ter228Tyr
ENST00000425614.3:c.1125G>C	ENSP00000387640.2:p.Ter375Tyr
ENST00000473881.2:c.*716G>C	ENSP00000486667.1:n.*716G>C
NM_144701.2:c.1890G>C	NP_653302.2:p.Ter630Tyr
XM_005270516.2:c.1128G>C	XP_005270573.1:p.Ter376Tyr
XM_011540789.1:c.1980G>C	XP_011539091.1:p.Ter660Tyr
XM_011540790.1:c.1890G>C	XP_011539092.1:p.Ter630Tyr
XM_011540791.1:c.1890G>C	XP_011539093.1:p.Ter630Tyr
XM_011540790.3:c.1890G>C	XP_011539092.1:p.Ter630Tyr
XM_011540791.3:c.1890G>C	XP_011539093.1:p.Ter630Tyr
NM_144701.3:c.1890G>C MANE Select	NP_653302.2:p.Ter630Tyr