Canonical Allele Identifier: CA507947778

Gene: APOE

Linked Data

• gnomAD v4: 19-44909199-G-A
• MyVariant Identifiers: chr19:g.45412456G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44909199G>A , CM000681.2:g.44909199G>A	GRCh38
NC_000019.9:g.45412456G>A , CM000681.1:g.45412456G>A	GRCh37
NC_000019.8:g.50104296G>A	NCBI36
NG_007084.2:g.8418G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252486.9:c.903G>A MANE Select	ENSP00000252486.3:p.Val301=
ENST00000252486.8:c.903G>A	ENSP00000252486.3:p.Val301=
NM_000041.3:c.903G>A	NP_000032.1:p.Val301=
NM_001302688.1:c.981G>A	NP_001289617.1:p.Val327=
NM_001302689.1:c.903G>A	NP_001289618.1:p.Val301=
NM_001302690.1:c.903G>A	NP_001289619.1:p.Val301=
NM_001302691.1:c.903G>A	NP_001289620.1:p.Val301=
NM_000041.4:c.903G>A MANE Select	NP_000032.1:p.Val301=
NM_001302688.2:c.981G>A	NP_001289617.1:p.Val327=
NM_001302689.2:c.903G>A	NP_001289618.1:p.Val301=
NM_001302691.2:c.903G>A	NP_001289620.1:p.Val301=
NM_001302690.2:c.903G>A	NP_001289619.1:p.Val301=