Canonical Allele Identifier: CA1192531883

Gene: NOTCH2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119967573C= , CM000663.2:g.119967573C=	GRCh38
NC_000001.10:g.120510196C= , CM000663.1:g.120510196C=	GRCh37
NC_000001.9:g.120311719C=	NCBI36
NG_008163.1:g.107081G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256646.7:c.1313G= MANE Select	ENSP00000256646.2:p.Gly438=
ENST00000640021.1:c.533G=	ENSP00000492223.1:n.533G=
ENST00000256646.6:c.1313G=	ENSP00000256646.2:p.Gly438=
ENST00000479412.2:n.1451G=
ENST00000579475.7:c.1196G=	ENSP00000477065.2:p.Gly399=
NM_001200001.1:c.1313G=	NP_001186930.1:p.Gly438=
NM_024408.3:c.1313G=	NP_077719.2:p.Gly438=
XM_005270901.2:c.1196G=	XP_005270958.1:p.Gly399=
XM_011541519.1:c.1301G=	XP_011539821.1:p.Gly434=
XM_011541520.1:c.1196G=	XP_011539822.1:p.Gly399=
NM_024408.4:c.1313G= MANE Select	NP_077719.2:p.Gly438=
NM_001200001.2:c.1313G=	NP_001186930.1:p.Gly438=