Canonical Allele Identifier: CA507947554

Gene: APOE

Linked Data

• MyVariant Identifiers: chr19:g.45412216A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44908959A>T , CM000681.2:g.44908959A>T	GRCh38
NC_000019.9:g.45412216A>T , CM000681.1:g.45412216A>T	GRCh37
NC_000019.8:g.50104056A>T	NCBI36
NG_007084.2:g.8178A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000252486.9:c.663A>T MANE Select	ENSP00000252486.3:p.Leu221=
ENST00000252486.8:c.663A>T	ENSP00000252486.3:p.Leu221=
ENST00000434152.5:c.741A>T	ENSP00000413653.2:p.Leu247=
NM_000041.3:c.663A>T	NP_000032.1:p.Leu221=
NM_001302688.1:c.741A>T	NP_001289617.1:p.Leu247=
NM_001302689.1:c.663A>T	NP_001289618.1:p.Leu221=
NM_001302690.1:c.663A>T	NP_001289619.1:p.Leu221=
NM_001302691.1:c.663A>T	NP_001289620.1:p.Leu221=
NM_000041.4:c.663A>T MANE Select	NP_000032.1:p.Leu221=
NM_001302688.2:c.741A>T	NP_001289617.1:p.Leu247=
NM_001302689.2:c.663A>T	NP_001289618.1:p.Leu221=
NM_001302691.2:c.663A>T	NP_001289620.1:p.Leu221=
NM_001302690.2:c.663A>T	NP_001289619.1:p.Leu221=