Canonical Allele Identifier: CA041327
Gene: APOE HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 440842
ClinVar RCV Id: RCV000019453
dbSNP Id: rs201672011

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44907807G>A , CM000681.2:g.44907807G>A GRCh38
NC_000019.9:g.45411064G>A , CM000681.1:g.45411064G>A GRCh37
NC_000019.8:g.50102904G>A NCBI36
NG_007084.2:g.7026G>A

Transcript Alleles

HGVS Amino-acid change
NM_000041.3:c.91G>A VV NP_000032.1:p.Glu31Lys
NM_001302688.1:c.169G>A VV NP_001289617.1:p.Glu57Lys
NM_001302689.1:c.91G>A VV NP_001289618.1:p.Glu31Lys
NM_001302690.1:c.91G>A VV NP_001289619.1:p.Glu31Lys
NM_001302691.1:c.91G>A VV NP_001289620.1:p.Glu31Lys
ENST00000252486.8:c.91G>A ENSP00000252486.3:p.Glu31Lys
ENST00000425718.1:c.91G>A ENSP00000410423.1:p.Glu31Lys
ENST00000434152.5:c.169G>A ENSP00000413653.2:p.Glu57Lys
ENST00000446996.5:c.91G>A ENSP00000413135.1:p.Glu31Lys