Canonical Allele Identifier: CA2739619537
Gene: APOE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44905825T>G , CM000681.2:g.44905825T>G GRCh38
NC_000019.9:g.45409082T>G , CM000681.1:g.45409082T>G GRCh37
NC_000019.8:g.50100922T>G NCBI36
NG_007084.2:g.5044T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252486.9:c.-40T>G MANE Select ENSP00000252486.3:n.-40T>G
ENST00000252486.8:c.-40T>G ENSP00000252486.3:n.-40T>G
ENST00000434152.5:c.-44T>G ENSP00000413653.2:n.-44T>G
ENST00000446996.5:c.-55T>G ENSP00000413135.1:n.-55T>G
ENST00000485628.2:n.30T>G
NM_000041.3:c.-40T>G NP_000032.1:n.-40T>G
NM_001302688.1:c.-44T>G NP_001289617.1:n.-44T>G
NM_001302691.1:c.-55T>G NP_001289620.1:n.-55T>G
NM_000041.4:c.-40T>G MANE Select NP_000032.1:n.-40T>G
NM_001302688.2:c.-44T>G NP_001289617.1:n.-44T>G
NM_001302691.2:c.-55T>G NP_001289620.1:n.-55T>G