Canonical Allele Identifier: CA1192514442
Gene: NOTCH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.119915555C= , CM000663.2:g.119915555C= GRCh38
NC_000001.10:g.120458178C= , CM000663.1:g.120458178C= GRCh37
NC_000001.9:g.120259701C= NCBI36
NG_008163.1:g.159099G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256646.7:c.7167G= MANE Select ENSP00000256646.2:p.Gln2389=
ENST00000256646.6:c.7167G= ENSP00000256646.2:p.Gln2389=
NM_024408.3:c.7167G= NP_077719.2:p.Gln2389=
XM_005270901.2:c.7050G= XP_005270958.1:p.Gln2350=
XM_011541519.1:c.7155G= XP_011539821.1:p.Gln2385=
XM_011541520.1:c.7050G= XP_011539822.1:p.Gln2350=
NM_024408.4:c.7167G= MANE Select NP_077719.2:p.Gln2389=