Canonical Allele Identifier: CA418438832
Gene: IL23R HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.67724796A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67259113A>T , CM000663.2:g.67259113A>T GRCh38
NC_000001.10:g.67724796A>T , CM000663.1:g.67724796A>T GRCh37
NC_000001.9:g.67497384A>T NCBI36
NG_011498.1:g.97628A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000697149.1:c.1714A>T ENSP00000513138.1:n.1714A>T
ENST00000697150.1:c.1772A>T ENSP00000513139.1:n.1772A>T
ENST00000697151.1:c.1705A>T ENSP00000513140.1:n.1705A>T
ENST00000697164.1:c.1785A>T ENSP00000513153.1:p.Ser595=
ENST00000697165.1:c.1572A>T ENSP00000513154.1:p.Ser524=
ENST00000347310.10:c.1875A>T MANE Select ENSP00000321345.5:p.Ser625=
ENST00000637002.1:c.1266A>T ENSP00000490340.1:p.Ser422=
ENST00000347310.9:c.1875A>T ENSP00000321345.5:p.Ser625=
ENST00000395227.2:c.669A>T ENSP00000378652.2:p.Ser223=
ENST00000425614.3:c.1110A>T ENSP00000387640.2:p.Ser370=
ENST00000473881.2:c.*701A>T ENSP00000486667.1:n.*701A>T
NM_144701.2:c.1875A>T NP_653302.2:p.Ser625=
XM_005270516.2:c.1113A>T XP_005270573.1:p.Ser371=
XM_011540789.1:c.1965A>T XP_011539091.1:p.Ser655=
XM_011540790.1:c.1875A>T XP_011539092.1:p.Ser625=
XM_011540791.1:c.1875A>T XP_011539093.1:p.Ser625=
XM_011540790.3:c.1875A>T XP_011539092.1:p.Ser625=
XM_011540791.3:c.1875A>T XP_011539093.1:p.Ser625=
XR_001736993.1:n.1955A>T
NM_144701.3:c.1875A>T MANE Select NP_653302.2:p.Ser625=