Canonical Allele Identifier: CA2585713779

Gene: APOE

Linked Data

• gnomAD v4: 19-44905830-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44905830C>G , CM000681.2:g.44905830C>G	GRCh38
NC_000019.9:g.45409087C>G , CM000681.1:g.45409087C>G	GRCh37
NC_000019.8:g.50100927C>G	NCBI36
NG_007084.2:g.5049C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252486.9:c.-35C>G MANE Select	ENSP00000252486.3:n.-35C>G
ENST00000252486.8:c.-35C>G	ENSP00000252486.3:n.-35C>G
ENST00000434152.5:c.-39C>G	ENSP00000413653.2:n.-39C>G
ENST00000446996.5:c.-50C>G	ENSP00000413135.1:n.-50C>G
ENST00000485628.2:n.35C>G
NM_000041.3:c.-35C>G	NP_000032.1:n.-35C>G
NM_001302688.1:c.-39C>G	NP_001289617.1:n.-39C>G
NM_001302691.1:c.-50C>G	NP_001289620.1:n.-50C>G
NM_000041.4:c.-35C>G MANE Select	NP_000032.1:n.-35C>G
NM_001302688.2:c.-39C>G	NP_001289617.1:n.-39C>G
NM_001302691.2:c.-50C>G	NP_001289620.1:n.-50C>G