Canonical Allele Identifier: CA2338168132

Gene: APOE

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44909214C= , CM000681.2:g.44909214C=	GRCh38
NC_000019.9:g.45412471C= , CM000681.1:g.45412471C=	GRCh37
NC_000019.8:g.50104311C=	NCBI36
NG_007084.2:g.8433C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252486.9:c.918C= MANE Select	ENSP00000252486.3:p.Gly306=
ENST00000252486.8:c.918C=	ENSP00000252486.3:p.Gly306=
NM_000041.3:c.918C=	NP_000032.1:p.Gly306=
NM_001302688.1:c.996C=	NP_001289617.1:p.Gly332=
NM_001302689.1:c.918C=	NP_001289618.1:p.Gly306=
NM_001302690.1:c.918C=	NP_001289619.1:p.Gly306=
NM_001302691.1:c.918C=	NP_001289620.1:p.Gly306=
NM_000041.4:c.918C= MANE Select	NP_000032.1:p.Gly306=
NM_001302688.2:c.996C=	NP_001289617.1:p.Gly332=
NM_001302689.2:c.918C=	NP_001289618.1:p.Gly306=
NM_001302691.2:c.918C=	NP_001289620.1:p.Gly306=
NM_001302690.2:c.918C=	NP_001289619.1:p.Gly306=