Canonical Allele Identifier: CA2585715587

Gene: APOE

Linked Data

• gnomAD v4: 19-44909363-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44909363A>G , CM000681.2:g.44909363A>G	GRCh38
NC_000019.9:g.45412620A>G , CM000681.1:g.45412620A>G	GRCh37
NC_000019.8:g.50104460A>G	NCBI36
NG_007084.2:g.8582A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252486.9:c.*113A>G MANE Select	ENSP00000252486.3:n.*113A>G
ENST00000252486.8:c.*113A>G	ENSP00000252486.3:n.*113A>G
NM_000041.3:c.*113A>G	NP_000032.1:n.*113A>G
NM_001302688.1:c.*113A>G	NP_001289617.1:n.*113A>G
NM_001302689.1:c.*113A>G	NP_001289618.1:n.*113A>G
NM_001302690.1:c.*113A>G	NP_001289619.1:n.*113A>G
NM_001302691.1:c.*113A>G	NP_001289620.1:n.*113A>G
NM_000041.4:c.*113A>G MANE Select	NP_000032.1:n.*113A>G
NM_001302688.2:c.*113A>G	NP_001289617.1:n.*113A>G
NM_001302689.2:c.*113A>G	NP_001289618.1:n.*113A>G
NM_001302691.2:c.*113A>G	NP_001289620.1:n.*113A>G
NM_001302690.2:c.*113A>G	NP_001289619.1:n.*113A>G