Canonical Allele Identifier: CA340728779

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724507A>C (hg19) ; chr1:g.67258824A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258824A>C , CM000663.2:g.67258824A>C	GRCh38
NC_000001.10:g.67724507A>C , CM000663.1:g.67724507A>C	GRCh37
NC_000001.9:g.67497095A>C	NCBI36
NG_011498.1:g.97339A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1425A>C	ENSP00000513138.1:n.1425A>C
ENST00000697150.1:c.1483A>C	ENSP00000513139.1:n.1483A>C
ENST00000697151.1:c.1416A>C	ENSP00000513140.1:n.1416A>C
ENST00000697164.1:c.1496A>C	ENSP00000513153.1:p.Asn499Thr
ENST00000697165.1:c.1283A>C	ENSP00000513154.1:p.Asn428Thr
ENST00000347310.10:c.1586A>C MANE Select	ENSP00000321345.5:p.Asn529Thr
ENST00000637002.1:c.977A>C	ENSP00000490340.1:p.Asn326Thr
ENST00000347310.9:c.1586A>C	ENSP00000321345.5:p.Asn529Thr
ENST00000395227.2:c.380A>C	ENSP00000378652.2:p.Asn127Thr
ENST00000425614.3:c.821A>C	ENSP00000387640.2:p.Asn274Thr
ENST00000473881.2:c.*412A>C	ENSP00000486667.1:n.*412A>C
NM_144701.2:c.1586A>C	NP_653302.2:p.Asn529Thr
XM_005270516.2:c.824A>C	XP_005270573.1:p.Asn275Thr
XM_011540789.1:c.1676A>C	XP_011539091.1:p.Asn559Thr
XM_011540790.1:c.1586A>C	XP_011539092.1:p.Asn529Thr
XM_011540791.1:c.1586A>C	XP_011539093.1:p.Asn529Thr
XM_011540790.3:c.1586A>C	XP_011539092.1:p.Asn529Thr
XM_011540791.3:c.1586A>C	XP_011539093.1:p.Asn529Thr
XR_001736993.1:n.1666A>C
NM_144701.3:c.1586A>C MANE Select	NP_653302.2:p.Asn529Thr