Canonical Allele Identifier: CA882661582

Gene: APOE

Linked Data

• dbSNP Id: rs1351486646
• MyVariant Identifiers: chr19:g.45409077G>A (hg19) ; chr19:g.44905820G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44905820G>A , CM000681.2:g.44905820G>A	GRCh38
NC_000019.9:g.45409077G>A , CM000681.1:g.45409077G>A	GRCh37
NC_000019.8:g.50100917G>A	NCBI36
NG_007084.2:g.5039G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252486.9:c.-45G>A MANE Select	ENSP00000252486.3:n.-45G>A
ENST00000252486.8:c.-45G>A	ENSP00000252486.3:n.-45G>A
ENST00000434152.5:c.-49G>A	ENSP00000413653.2:n.-49G>A
ENST00000446996.5:c.-60G>A	ENSP00000413135.1:n.-60G>A
ENST00000485628.2:n.25G>A
NM_000041.3:c.-45G>A	NP_000032.1:n.-45G>A
NM_001302688.1:c.-49G>A	NP_001289617.1:n.-49G>A
NM_001302691.1:c.-60G>A	NP_001289620.1:n.-60G>A
NM_000041.4:c.-45G>A MANE Select	NP_000032.1:n.-45G>A
NM_001302688.2:c.-49G>A	NP_001289617.1:n.-49G>A
NM_001302691.2:c.-60G>A	NP_001289620.1:n.-60G>A