Canonical Allele Identifier: CA2585715602

Gene: APOE

Linked Data

• gnomAD v4: 19-44909389-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44909389A>G , CM000681.2:g.44909389A>G	GRCh38
NC_000019.9:g.45412646A>G , CM000681.1:g.45412646A>G	GRCh37
NC_000019.8:g.50104486A>G	NCBI36
NG_007084.2:g.8608A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252486.9:c.*139A>G MANE Select	ENSP00000252486.3:n.*139A>G
ENST00000252486.8:c.*139A>G	ENSP00000252486.3:n.*139A>G
NM_000041.3:c.*139A>G	NP_000032.1:n.*139A>G
NM_001302688.1:c.*139A>G	NP_001289617.1:n.*139A>G
NM_001302689.1:c.*139A>G	NP_001289618.1:n.*139A>G
NM_001302690.1:c.*139A>G	NP_001289619.1:n.*139A>G
NM_001302691.1:c.*139A>G	NP_001289620.1:n.*139A>G
NM_000041.4:c.*139A>G MANE Select	NP_000032.1:n.*139A>G
NM_001302688.2:c.*139A>G	NP_001289617.1:n.*139A>G
NM_001302689.2:c.*139A>G	NP_001289618.1:n.*139A>G
NM_001302691.2:c.*139A>G	NP_001289620.1:n.*139A>G
NM_001302690.2:c.*139A>G	NP_001289619.1:n.*139A>G