Canonical Allele Identifier: CA2338168220

Gene: APOE

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44909351G= , CM000681.2:g.44909351G=	GRCh38
NC_000019.9:g.45412608G= , CM000681.1:g.45412608G=	GRCh37
NC_000019.8:g.50104448G=	NCBI36
NG_007084.2:g.8570G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252486.9:c.*101G= MANE Select	ENSP00000252486.3:n.*101G=
ENST00000252486.8:c.*101G=	ENSP00000252486.3:n.*101G=
NM_000041.3:c.*101G=	NP_000032.1:n.*101G=
NM_001302688.1:c.*101G=	NP_001289617.1:n.*101G=
NM_001302689.1:c.*101G=	NP_001289618.1:n.*101G=
NM_001302690.1:c.*101G=	NP_001289619.1:n.*101G=
NM_001302691.1:c.*101G=	NP_001289620.1:n.*101G=
NM_000041.4:c.*101G= MANE Select	NP_000032.1:n.*101G=
NM_001302688.2:c.*101G=	NP_001289617.1:n.*101G=
NM_001302689.2:c.*101G=	NP_001289618.1:n.*101G=
NM_001302691.2:c.*101G=	NP_001289620.1:n.*101G=
NM_001302690.2:c.*101G=	NP_001289619.1:n.*101G=