Canonical Allele Identifier: CA340730219
Community Standard Title: NM_144701.3(IL23R):c.1889A>C (p.Ter630Ser)
Gene: IL23R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67259127A>C , CM000663.2:g.67259127A>C GRCh38
NC_000001.10:g.67724810A>C , CM000663.1:g.67724810A>C GRCh37
NC_000001.9:g.67497398A>C NCBI36
NG_011498.1:g.97642A>C

Transcript Alleles

HGVS Amino-acid Change
NM_144701.3:c.1889A>C MANE Select NP_653302.2:p.Ter630Ser
ENST00000347310.10:c.1889A>C MANE Select ENSP00000321345.5:p.Ter630Ser
NM_144701.2:c.1889A>C NP_653302.2:p.Ter630Ser
ENST00000347310.9:c.1889A>C ENSP00000321345.5:p.Ter630Ser
ENST00000395227.2:c.683A>C ENSP00000378652.2:p.Ter228Ser
ENST00000425614.3:c.1124A>C ENSP00000387640.2:p.Ter375Ser
ENST00000473881.2:c.*715A>C ENSP00000486667.1:n.*715A>C
ENST00000637002.1:c.1280A>C ENSP00000490340.1:p.Ter427Ser
ENST00000697164.1:c.1799A>C ENSP00000513153.1:p.Ter600Ser
ENST00000697165.1:c.1586A>C ENSP00000513154.1:p.Ter529Ser
XM_005270516.2:c.1127A>C XP_005270573.1:p.Ter376Ser
XM_011540789.1:c.1979A>C XP_011539091.1:p.Ter660Ser
XM_011540790.1:c.1889A>C XP_011539092.1:p.Ter630Ser
XM_011540790.3:c.1889A>C XP_011539092.1:p.Ter630Ser
XM_011540791.1:c.1889A>C XP_011539093.1:p.Ter630Ser
XM_011540791.3:c.1889A>C XP_011539093.1:p.Ter630Ser