Canonical Allele Identifier: CA2739619539
Gene: APOE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44905828T>A , CM000681.2:g.44905828T>A GRCh38
NC_000019.9:g.45409085T>A , CM000681.1:g.45409085T>A GRCh37
NC_000019.8:g.50100925T>A NCBI36
NG_007084.2:g.5047T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252486.9:c.-37T>A MANE Select ENSP00000252486.3:n.-37T>A
ENST00000252486.8:c.-37T>A ENSP00000252486.3:n.-37T>A
ENST00000434152.5:c.-41T>A ENSP00000413653.2:n.-41T>A
ENST00000446996.5:c.-52T>A ENSP00000413135.1:n.-52T>A
ENST00000485628.2:n.33T>A
NM_000041.3:c.-37T>A NP_000032.1:n.-37T>A
NM_001302688.1:c.-41T>A NP_001289617.1:n.-41T>A
NM_001302691.1:c.-52T>A NP_001289620.1:n.-52T>A
NM_000041.4:c.-37T>A MANE Select NP_000032.1:n.-37T>A
NM_001302688.2:c.-41T>A NP_001289617.1:n.-41T>A
NM_001302691.2:c.-52T>A NP_001289620.1:n.-52T>A