Canonical Allele Identifier: CA418438793

Gene: IL23R

Linked Data

• gnomAD v4: 1-67259062-T-C
• COSMIC: COSM4009649 ; COSM4009650
• MyVariant Identifiers: chr1:g.67724745T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259062T>C , CM000663.2:g.67259062T>C	GRCh38
NC_000001.10:g.67724745T>C , CM000663.1:g.67724745T>C	GRCh37
NC_000001.9:g.67497333T>C	NCBI36
NG_011498.1:g.97577T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1663T>C	ENSP00000513138.1:n.1663T>C
ENST00000697150.1:c.1721T>C	ENSP00000513139.1:n.1721T>C
ENST00000697151.1:c.1654T>C	ENSP00000513140.1:n.1654T>C
ENST00000697164.1:c.1734T>C	ENSP00000513153.1:p.Ile578=
ENST00000697165.1:c.1521T>C	ENSP00000513154.1:p.Ile507=
ENST00000347310.10:c.1824T>C MANE Select	ENSP00000321345.5:p.Ile608=
ENST00000637002.1:c.1215T>C	ENSP00000490340.1:p.Ile405=
ENST00000347310.9:c.1824T>C	ENSP00000321345.5:p.Ile608=
ENST00000395227.2:c.618T>C	ENSP00000378652.2:p.Ile206=
ENST00000425614.3:c.1059T>C	ENSP00000387640.2:p.Ile353=
ENST00000473881.2:c.*650T>C	ENSP00000486667.1:n.*650T>C
NM_144701.2:c.1824T>C	NP_653302.2:p.Ile608=
XM_005270516.2:c.1062T>C	XP_005270573.1:p.Ile354=
XM_011540789.1:c.1914T>C	XP_011539091.1:p.Ile638=
XM_011540790.1:c.1824T>C	XP_011539092.1:p.Ile608=
XM_011540791.1:c.1824T>C	XP_011539093.1:p.Ile608=
XM_011540790.3:c.1824T>C	XP_011539092.1:p.Ile608=
XM_011540791.3:c.1824T>C	XP_011539093.1:p.Ile608=
XR_001736993.1:n.1904T>C
NM_144701.3:c.1824T>C MANE Select	NP_653302.2:p.Ile608=