Canonical Allele Identifier: CA308885751

Gene: APOE

Linked Data

• dbSNP Id: rs985595848
• gnomAD v4: 19-44908782-G-A
• MyVariant Identifiers: chr19:g.45412039G>A (hg19) ; chr19:g.44908782G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44908782G>A , CM000681.2:g.44908782G>A	GRCh38
NC_000019.9:g.45412039G>A , CM000681.1:g.45412039G>A	GRCh37
NC_000019.8:g.50103879G>A	NCBI36
NG_007084.2:g.8001G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252486.9:c.486G>A MANE Select	ENSP00000252486.3:p.Leu162=
ENST00000252486.8:c.486G>A	ENSP00000252486.3:p.Leu162=
ENST00000425718.1:c.486G>A	ENSP00000410423.1:p.Leu162=
ENST00000434152.5:c.564G>A	ENSP00000413653.2:p.Leu188=
ENST00000446996.5:c.486G>A	ENSP00000413135.1:p.Leu162=
NM_000041.3:c.486G>A	NP_000032.1:p.Leu162=
NM_001302688.1:c.564G>A	NP_001289617.1:p.Leu188=
NM_001302689.1:c.486G>A	NP_001289618.1:p.Leu162=
NM_001302690.1:c.486G>A	NP_001289619.1:p.Leu162=
NM_001302691.1:c.486G>A	NP_001289620.1:p.Leu162=
NM_000041.4:c.486G>A MANE Select	NP_000032.1:p.Leu162=
NM_001302688.2:c.564G>A	NP_001289617.1:p.Leu188=
NM_001302689.2:c.486G>A	NP_001289618.1:p.Leu162=
NM_001302691.2:c.486G>A	NP_001289620.1:p.Leu162=
NM_001302690.2:c.486G>A	NP_001289619.1:p.Leu162=