Canonical Allele Identifier: CA340729338

Gene: IL23R

Linked Data

• dbSNP Id: rs1344309440
• gnomAD v3: 1-67258946-G-C
• gnomAD v4: 1-67258946-G-C
• MyVariant Identifiers: chr1:g.67724629G>C (hg19) ; chr1:g.67258946G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258946G>C , CM000663.2:g.67258946G>C	GRCh38
NC_000001.10:g.67724629G>C , CM000663.1:g.67724629G>C	GRCh37
NC_000001.9:g.67497217G>C	NCBI36
NG_011498.1:g.97461G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1547G>C	ENSP00000513138.1:n.1547G>C
ENST00000697150.1:c.1605G>C	ENSP00000513139.1:n.1605G>C
ENST00000697151.1:c.1538G>C	ENSP00000513140.1:n.1538G>C
ENST00000697164.1:c.1618G>C	ENSP00000513153.1:p.Glu540Gln
ENST00000697165.1:c.1405G>C	ENSP00000513154.1:p.Glu469Gln
ENST00000347310.10:c.1708G>C MANE Select	ENSP00000321345.5:p.Glu570Gln
ENST00000637002.1:c.1099G>C	ENSP00000490340.1:p.Glu367Gln
ENST00000347310.9:c.1708G>C	ENSP00000321345.5:p.Glu570Gln
ENST00000395227.2:c.502G>C	ENSP00000378652.2:p.Glu168Gln
ENST00000425614.3:c.943G>C	ENSP00000387640.2:p.Glu315Gln
ENST00000473881.2:c.*534G>C	ENSP00000486667.1:n.*534G>C
NM_144701.2:c.1708G>C	NP_653302.2:p.Glu570Gln
XM_005270516.2:c.946G>C	XP_005270573.1:p.Glu316Gln
XM_011540789.1:c.1798G>C	XP_011539091.1:p.Glu600Gln
XM_011540790.1:c.1708G>C	XP_011539092.1:p.Glu570Gln
XM_011540791.1:c.1708G>C	XP_011539093.1:p.Glu570Gln
XM_011540790.3:c.1708G>C	XP_011539092.1:p.Glu570Gln
XM_011540791.3:c.1708G>C	XP_011539093.1:p.Glu570Gln
XR_001736993.1:n.1788G>C
NM_144701.3:c.1708G>C MANE Select	NP_653302.2:p.Glu570Gln