Canonical Allele Identifier: CA2739619544
Gene: APOE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44905835G>T , CM000681.2:g.44905835G>T GRCh38
NC_000019.9:g.45409092G>T , CM000681.1:g.45409092G>T GRCh37
NC_000019.8:g.50100932G>T NCBI36
NG_007084.2:g.5054G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252486.9:c.-30G>T MANE Select ENSP00000252486.3:n.-30G>T
ENST00000252486.8:c.-30G>T ENSP00000252486.3:n.-30G>T
ENST00000434152.5:c.-34G>T ENSP00000413653.2:n.-34G>T
ENST00000446996.5:c.-45G>T ENSP00000413135.1:n.-45G>T
ENST00000485628.2:n.40G>T
NM_000041.3:c.-30G>T NP_000032.1:n.-30G>T
NM_001302688.1:c.-34G>T NP_001289617.1:n.-34G>T
NM_001302691.1:c.-45G>T NP_001289620.1:n.-45G>T
NM_000041.4:c.-30G>T MANE Select NP_000032.1:n.-30G>T
NM_001302688.2:c.-34G>T NP_001289617.1:n.-34G>T
NM_001302691.2:c.-45G>T NP_001289620.1:n.-45G>T