Canonical Allele Identifier: CA1192531863
Gene: NOTCH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.119967477G= , CM000663.2:g.119967477G= GRCh38
NC_000001.10:g.120510100G= , CM000663.1:g.120510100G= GRCh37
NC_000001.9:g.120311623G= NCBI36
NG_008163.1:g.107177C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256646.7:c.1409C= MANE Select ENSP00000256646.2:p.Thr470=
ENST00000640021.1:c.629C= ENSP00000492223.1:n.629C=
ENST00000256646.6:c.1409C= ENSP00000256646.2:p.Thr470=
ENST00000479412.2:n.1547C=
ENST00000579475.7:c.1292C= ENSP00000477065.2:p.Thr431=
NM_001200001.1:c.1409C= NP_001186930.1:p.Thr470=
NM_024408.3:c.1409C= NP_077719.2:p.Thr470=
XM_005270901.2:c.1292C= XP_005270958.1:p.Thr431=
XM_011541519.1:c.1397C= XP_011539821.1:p.Thr466=
XM_011541520.1:c.1292C= XP_011539822.1:p.Thr431=
NM_024408.4:c.1409C= MANE Select NP_077719.2:p.Thr470=
NM_001200001.2:c.1409C= NP_001186930.1:p.Thr470=