Canonical Allele Identifier: CA418438748

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724508T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258825T>C , CM000663.2:g.67258825T>C	GRCh38
NC_000001.10:g.67724508T>C , CM000663.1:g.67724508T>C	GRCh37
NC_000001.9:g.67497096T>C	NCBI36
NG_011498.1:g.97340T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1426T>C	ENSP00000513138.1:n.1426T>C
ENST00000697150.1:c.1484T>C	ENSP00000513139.1:n.1484T>C
ENST00000697151.1:c.1417T>C	ENSP00000513140.1:n.1417T>C
ENST00000697164.1:c.1497T>C	ENSP00000513153.1:p.Asn499=
ENST00000697165.1:c.1284T>C	ENSP00000513154.1:p.Asn428=
ENST00000347310.10:c.1587T>C MANE Select	ENSP00000321345.5:p.Asn529=
ENST00000637002.1:c.978T>C	ENSP00000490340.1:p.Asn326=
ENST00000347310.9:c.1587T>C	ENSP00000321345.5:p.Asn529=
ENST00000395227.2:c.381T>C	ENSP00000378652.2:p.Asn127=
ENST00000425614.3:c.822T>C	ENSP00000387640.2:p.Asn274=
ENST00000473881.2:c.*413T>C	ENSP00000486667.1:n.*413T>C
NM_144701.2:c.1587T>C	NP_653302.2:p.Asn529=
XM_005270516.2:c.825T>C	XP_005270573.1:p.Asn275=
XM_011540789.1:c.1677T>C	XP_011539091.1:p.Asn559=
XM_011540790.1:c.1587T>C	XP_011539092.1:p.Asn529=
XM_011540791.1:c.1587T>C	XP_011539093.1:p.Asn529=
XM_011540790.3:c.1587T>C	XP_011539092.1:p.Asn529=
XM_011540791.3:c.1587T>C	XP_011539093.1:p.Asn529=
XR_001736993.1:n.1667T>C
NM_144701.3:c.1587T>C MANE Select	NP_653302.2:p.Asn529=