Canonical Allele Identifier: CA406305528
Gene: APOE HGNC NCBI

Linked Data

dbSNP Id: rs1476757984

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44909131C>T , CM000681.2:g.44909131C>T GRCh38
NC_000019.9:g.45412388C>T , CM000681.1:g.45412388C>T GRCh37
NC_000019.8:g.50104228C>T NCBI36
NG_007084.2:g.8350C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252486.9:c.835C>T MANE Select ENSP00000252486.3:p.Leu279Phe
ENST00000252486.8:c.835C>T ENSP00000252486.3:p.Leu279Phe
NM_000041.3:c.835C>T NP_000032.1:p.Leu279Phe
NM_001302688.1:c.913C>T NP_001289617.1:p.Leu305Phe
NM_001302689.1:c.835C>T NP_001289618.1:p.Leu279Phe
NM_001302690.1:c.835C>T NP_001289619.1:p.Leu279Phe
NM_001302691.1:c.835C>T NP_001289620.1:p.Leu279Phe
NM_000041.4:c.835C>T MANE Select NP_000032.1:p.Leu279Phe
NM_001302688.2:c.913C>T NP_001289617.1:p.Leu305Phe
NM_001302689.2:c.835C>T NP_001289618.1:p.Leu279Phe
NM_001302691.2:c.835C>T NP_001289620.1:p.Leu279Phe
NM_001302690.2:c.835C>T NP_001289619.1:p.Leu279Phe