Canonical Allele Identifier: CA2338168238
Gene: APOE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44909392C= , CM000681.2:g.44909392C= GRCh38
NC_000019.9:g.45412649C= , CM000681.1:g.45412649C= GRCh37
NC_000019.8:g.50104489C= NCBI36
NG_007084.2:g.8611C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252486.9:c.*142C= MANE Select ENSP00000252486.3:n.*142C=
ENST00000252486.8:c.*142C= ENSP00000252486.3:n.*142C=
NM_000041.3:c.*142C= NP_000032.1:n.*142C=
NM_001302688.1:c.*142C= NP_001289617.1:n.*142C=
NM_001302689.1:c.*142C= NP_001289618.1:n.*142C=
NM_001302690.1:c.*142C= NP_001289619.1:n.*142C=
NM_001302691.1:c.*142C= NP_001289620.1:n.*142C=
NM_000041.4:c.*142C= MANE Select NP_000032.1:n.*142C=
NM_001302688.2:c.*142C= NP_001289617.1:n.*142C=
NM_001302689.2:c.*142C= NP_001289618.1:n.*142C=
NM_001302691.2:c.*142C= NP_001289620.1:n.*142C=
NM_001302690.2:c.*142C= NP_001289619.1:n.*142C=