Canonical Allele Identifier: CA1192514441
Gene: NOTCH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.119915554G= , CM000663.2:g.119915554G= GRCh38
NC_000001.10:g.120458177G= , CM000663.1:g.120458177G= GRCh37
NC_000001.9:g.120259700G= NCBI36
NG_008163.1:g.159100C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256646.7:c.7168C= MANE Select ENSP00000256646.2:p.His2390=
ENST00000256646.6:c.7168C= ENSP00000256646.2:p.His2390=
NM_024408.3:c.7168C= NP_077719.2:p.His2390=
XM_005270901.2:c.7051C= XP_005270958.1:p.His2351=
XM_011541519.1:c.7156C= XP_011539821.1:p.His2386=
XM_011541520.1:c.7051C= XP_011539822.1:p.His2351=
NM_024408.4:c.7168C= MANE Select NP_077719.2:p.His2390=