Canonical Allele Identifier: CA340728908

Gene: IL23R

Linked Data

• gnomAD v4: 1-67258863-A-C
• MyVariant Identifiers: chr1:g.67724546A>C (hg19) ; chr1:g.67258863A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258863A>C , CM000663.2:g.67258863A>C	GRCh38
NC_000001.10:g.67724546A>C , CM000663.1:g.67724546A>C	GRCh37
NC_000001.9:g.67497134A>C	NCBI36
NG_011498.1:g.97378A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1464A>C	ENSP00000513138.1:n.1464A>C
ENST00000697150.1:c.1522A>C	ENSP00000513139.1:n.1522A>C
ENST00000697151.1:c.1455A>C	ENSP00000513140.1:n.1455A>C
ENST00000697164.1:c.1535A>C	ENSP00000513153.1:p.Asn512Thr
ENST00000697165.1:c.1322A>C	ENSP00000513154.1:p.Asn441Thr
ENST00000347310.10:c.1625A>C MANE Select	ENSP00000321345.5:p.Asn542Thr
ENST00000637002.1:c.1016A>C	ENSP00000490340.1:p.Asn339Thr
ENST00000347310.9:c.1625A>C	ENSP00000321345.5:p.Asn542Thr
ENST00000395227.2:c.419A>C	ENSP00000378652.2:p.Asn140Thr
ENST00000425614.3:c.860A>C	ENSP00000387640.2:p.Asn287Thr
ENST00000473881.2:c.*451A>C	ENSP00000486667.1:n.*451A>C
NM_144701.2:c.1625A>C	NP_653302.2:p.Asn542Thr
XM_005270516.2:c.863A>C	XP_005270573.1:p.Asn288Thr
XM_011540789.1:c.1715A>C	XP_011539091.1:p.Asn572Thr
XM_011540790.1:c.1625A>C	XP_011539092.1:p.Asn542Thr
XM_011540791.1:c.1625A>C	XP_011539093.1:p.Asn542Thr
XM_011540790.3:c.1625A>C	XP_011539092.1:p.Asn542Thr
XM_011540791.3:c.1625A>C	XP_011539093.1:p.Asn542Thr
XR_001736993.1:n.1705A>C
NM_144701.3:c.1625A>C MANE Select	NP_653302.2:p.Asn542Thr