Canonical Allele Identifier: CA2585715586

Gene: APOE

Linked Data

• gnomAD v4: 19-44909362-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44909362T>G , CM000681.2:g.44909362T>G	GRCh38
NC_000019.9:g.45412619T>G , CM000681.1:g.45412619T>G	GRCh37
NC_000019.8:g.50104459T>G	NCBI36
NG_007084.2:g.8581T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252486.9:c.*112T>G MANE Select	ENSP00000252486.3:n.*112T>G
ENST00000252486.8:c.*112T>G	ENSP00000252486.3:n.*112T>G
NM_000041.3:c.*112T>G	NP_000032.1:n.*112T>G
NM_001302688.1:c.*112T>G	NP_001289617.1:n.*112T>G
NM_001302689.1:c.*112T>G	NP_001289618.1:n.*112T>G
NM_001302690.1:c.*112T>G	NP_001289619.1:n.*112T>G
NM_001302691.1:c.*112T>G	NP_001289620.1:n.*112T>G
NM_000041.4:c.*112T>G MANE Select	NP_000032.1:n.*112T>G
NM_001302688.2:c.*112T>G	NP_001289617.1:n.*112T>G
NM_001302689.2:c.*112T>G	NP_001289618.1:n.*112T>G
NM_001302691.2:c.*112T>G	NP_001289620.1:n.*112T>G
NM_001302690.2:c.*112T>G	NP_001289619.1:n.*112T>G