Canonical Allele Identifier: CA2739619541
Gene: APOE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44905834A>T , CM000681.2:g.44905834A>T GRCh38
NC_000019.9:g.45409091A>T , CM000681.1:g.45409091A>T GRCh37
NC_000019.8:g.50100931A>T NCBI36
NG_007084.2:g.5053A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252486.9:c.-31A>T MANE Select ENSP00000252486.3:n.-31A>T
ENST00000252486.8:c.-31A>T ENSP00000252486.3:n.-31A>T
ENST00000434152.5:c.-35A>T ENSP00000413653.2:n.-35A>T
ENST00000446996.5:c.-46A>T ENSP00000413135.1:n.-46A>T
ENST00000485628.2:n.39A>T
NM_000041.3:c.-31A>T NP_000032.1:n.-31A>T
NM_001302688.1:c.-35A>T NP_001289617.1:n.-35A>T
NM_001302691.1:c.-46A>T NP_001289620.1:n.-46A>T
NM_000041.4:c.-31A>T MANE Select NP_000032.1:n.-31A>T
NM_001302688.2:c.-35A>T NP_001289617.1:n.-35A>T
NM_001302691.2:c.-46A>T NP_001289620.1:n.-46A>T