Canonical Allele Identifier: CA2338168233
Gene: APOE HGNC NCBI

Linked Data

dbSNP Id: rs1312338515

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44909381C>A , CM000681.2:g.44909381C>A GRCh38
NC_000019.9:g.45412638C>A , CM000681.1:g.45412638C>A GRCh37
NC_000019.8:g.50104478C>A NCBI36
NG_007084.2:g.8600C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252486.9:c.*131C>A MANE Select ENSP00000252486.3:n.*131C>A
ENST00000252486.8:c.*131C>A ENSP00000252486.3:n.*131C>A
NM_000041.3:c.*131C>A NP_000032.1:n.*131C>A
NM_001302688.1:c.*131C>A NP_001289617.1:n.*131C>A
NM_001302689.1:c.*131C>A NP_001289618.1:n.*131C>A
NM_001302690.1:c.*131C>A NP_001289619.1:n.*131C>A
NM_001302691.1:c.*131C>A NP_001289620.1:n.*131C>A
NM_000041.4:c.*131C>A MANE Select NP_000032.1:n.*131C>A
NM_001302688.2:c.*131C>A NP_001289617.1:n.*131C>A
NM_001302689.2:c.*131C>A NP_001289618.1:n.*131C>A
NM_001302691.2:c.*131C>A NP_001289620.1:n.*131C>A
NM_001302690.2:c.*131C>A NP_001289619.1:n.*131C>A