Canonical Allele Identifier: CA2338166381

Gene: APOE

Linked Data

• dbSNP Id: rs1476420254
• gnomAD v4: 19-44905814-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44905814G>A , CM000681.2:g.44905814G>A	GRCh38
NC_000019.9:g.45409071G>A , CM000681.1:g.45409071G>A	GRCh37
NC_000019.8:g.50100911G>A	NCBI36
NG_007084.2:g.5033G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000252486.9:c.-51G>A MANE Select	ENSP00000252486.3:n.-51G>A
ENST00000252486.8:c.-51G>A	ENSP00000252486.3:n.-51G>A
ENST00000434152.5:c.-55G>A	ENSP00000413653.2:n.-55G>A
ENST00000446996.5:c.-66G>A	ENSP00000413135.1:n.-66G>A
ENST00000485628.2:n.19G>A
NM_000041.3:c.-51G>A	NP_000032.1:n.-51G>A
NM_001302688.1:c.-55G>A	NP_001289617.1:n.-55G>A
NM_001302691.1:c.-66G>A	NP_001289620.1:n.-66G>A
NM_000041.4:c.-51G>A MANE Select	NP_000032.1:n.-51G>A
NM_001302688.2:c.-55G>A	NP_001289617.1:n.-55G>A
NM_001302691.2:c.-66G>A	NP_001289620.1:n.-66G>A