Canonical Allele Identifier: CA2739619529
Gene: APOE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44905818A>C , CM000681.2:g.44905818A>C GRCh38
NC_000019.9:g.45409075A>C , CM000681.1:g.45409075A>C GRCh37
NC_000019.8:g.50100915A>C NCBI36
NG_007084.2:g.5037A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000252486.9:c.-47A>C MANE Select ENSP00000252486.3:n.-47A>C
ENST00000252486.8:c.-47A>C ENSP00000252486.3:n.-47A>C
ENST00000434152.5:c.-51A>C ENSP00000413653.2:n.-51A>C
ENST00000446996.5:c.-62A>C ENSP00000413135.1:n.-62A>C
ENST00000485628.2:n.23A>C
NM_000041.3:c.-47A>C NP_000032.1:n.-47A>C
NM_001302688.1:c.-51A>C NP_001289617.1:n.-51A>C
NM_001302691.1:c.-62A>C NP_001289620.1:n.-62A>C
NM_000041.4:c.-47A>C MANE Select NP_000032.1:n.-47A>C
NM_001302688.2:c.-51A>C NP_001289617.1:n.-51A>C
NM_001302691.2:c.-62A>C NP_001289620.1:n.-62A>C