Canonical Allele Identifier: CA418438830
Gene: IL23R HGNC NCBI

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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