Canonical Allele Identifier: CA2338168030

Gene: APOE

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44909032C= , CM000681.2:g.44909032C=	GRCh38
NC_000019.9:g.45412289C= , CM000681.1:g.45412289C=	GRCh37
NC_000019.8:g.50104129C=	NCBI36
NG_007084.2:g.8251C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252486.9:c.736C= MANE Select	ENSP00000252486.3:p.Arg246=
ENST00000252486.8:c.736C=	ENSP00000252486.3:p.Arg246=
NM_000041.3:c.736C=	NP_000032.1:p.Arg246=
NM_001302688.1:c.814C=	NP_001289617.1:p.Arg272=
NM_001302689.1:c.736C=	NP_001289618.1:p.Arg246=
NM_001302690.1:c.736C=	NP_001289619.1:p.Arg246=
NM_001302691.1:c.736C=	NP_001289620.1:p.Arg246=
NM_000041.4:c.736C= MANE Select	NP_000032.1:p.Arg246=
NM_001302688.2:c.814C=	NP_001289617.1:p.Arg272=
NM_001302689.2:c.736C=	NP_001289618.1:p.Arg246=
NM_001302691.2:c.736C=	NP_001289620.1:p.Arg246=
NM_001302690.2:c.736C=	NP_001289619.1:p.Arg246=