Canonical Allele Identifier: CA2338168077
Gene: APOE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44909121C= , CM000681.2:g.44909121C= GRCh38
NC_000019.9:g.45412378C= , CM000681.1:g.45412378C= GRCh37
NC_000019.8:g.50104218C= NCBI36
NG_007084.2:g.8340C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252486.9:c.825C= MANE Select ENSP00000252486.3:p.Phe275=
ENST00000252486.8:c.825C= ENSP00000252486.3:p.Phe275=
NM_000041.3:c.825C= NP_000032.1:p.Phe275=
NM_001302688.1:c.903C= NP_001289617.1:p.Phe301=
NM_001302689.1:c.825C= NP_001289618.1:p.Phe275=
NM_001302690.1:c.825C= NP_001289619.1:p.Phe275=
NM_001302691.1:c.825C= NP_001289620.1:p.Phe275=
NM_000041.4:c.825C= MANE Select NP_000032.1:p.Phe275=
NM_001302688.2:c.903C= NP_001289617.1:p.Phe301=
NM_001302689.2:c.825C= NP_001289618.1:p.Phe275=
NM_001302691.2:c.825C= NP_001289620.1:p.Phe275=
NM_001302690.2:c.825C= NP_001289619.1:p.Phe275=