Canonical Allele Identifier: CA406305798
Gene: APOE HGNC NCBI

Linked Data

ClinVar Variation Id: 1765256
ClinVar RCV Id: RCV002376228
dbSNP Id: rs1367811482

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44909191G>C , CM000681.2:g.44909191G>C GRCh38
NC_000019.9:g.45412448G>C , CM000681.1:g.45412448G>C GRCh37
NC_000019.8:g.50104288G>C NCBI36
NG_007084.2:g.8410G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000252486.9:c.895G>C MANE Select ENSP00000252486.3:p.Glu299Gln
ENST00000252486.8:c.895G>C ENSP00000252486.3:p.Glu299Gln
NM_000041.3:c.895G>C NP_000032.1:p.Glu299Gln
NM_001302688.1:c.973G>C NP_001289617.1:p.Glu325Gln
NM_001302689.1:c.895G>C NP_001289618.1:p.Glu299Gln
NM_001302690.1:c.895G>C NP_001289619.1:p.Glu299Gln
NM_001302691.1:c.895G>C NP_001289620.1:p.Glu299Gln
NM_000041.4:c.895G>C MANE Select NP_000032.1:p.Glu299Gln
NM_001302688.2:c.973G>C NP_001289617.1:p.Glu325Gln
NM_001302689.2:c.895G>C NP_001289618.1:p.Glu299Gln
NM_001302691.2:c.895G>C NP_001289620.1:p.Glu299Gln
NM_001302690.2:c.895G>C NP_001289619.1:p.Glu299Gln