Canonical Allele Identifier: CA2338168233

Gene: APOE

Linked Data

• dbSNP Id: rs1312338515
• gnomAD v4: 19-44909381-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44909381C>A , CM000681.2:g.44909381C>A	GRCh38
NC_000019.9:g.45412638C>A , CM000681.1:g.45412638C>A	GRCh37
NC_000019.8:g.50104478C>A	NCBI36
NG_007084.2:g.8600C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252486.9:c.*131C>A MANE Select	ENSP00000252486.3:n.*131C>A
ENST00000252486.8:c.*131C>A	ENSP00000252486.3:n.*131C>A
NM_000041.3:c.*131C>A	NP_000032.1:n.*131C>A
NM_001302688.1:c.*131C>A	NP_001289617.1:n.*131C>A
NM_001302689.1:c.*131C>A	NP_001289618.1:n.*131C>A
NM_001302690.1:c.*131C>A	NP_001289619.1:n.*131C>A
NM_001302691.1:c.*131C>A	NP_001289620.1:n.*131C>A
NM_000041.4:c.*131C>A MANE Select	NP_000032.1:n.*131C>A
NM_001302688.2:c.*131C>A	NP_001289617.1:n.*131C>A
NM_001302689.2:c.*131C>A	NP_001289618.1:n.*131C>A
NM_001302691.2:c.*131C>A	NP_001289620.1:n.*131C>A
NM_001302690.2:c.*131C>A	NP_001289619.1:n.*131C>A