Canonical Allele Identifier: CA996247945
Gene: APOE HGNC NCBI

Linked Data

dbSNP Id: rs1969894013
gnomAD v3: 19-44909357-G-A
gnomAD v4: 19-44909357-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44909357G>A , CM000681.2:g.44909357G>A GRCh38
NC_000019.9:g.45412614G>A , CM000681.1:g.45412614G>A GRCh37
NC_000019.8:g.50104454G>A NCBI36
NG_007084.2:g.8576G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252486.9:c.*107G>A MANE Select ENSP00000252486.3:n.*107G>A
ENST00000252486.8:c.*107G>A ENSP00000252486.3:n.*107G>A
NM_000041.3:c.*107G>A NP_000032.1:n.*107G>A
NM_001302688.1:c.*107G>A NP_001289617.1:n.*107G>A
NM_001302689.1:c.*107G>A NP_001289618.1:n.*107G>A
NM_001302690.1:c.*107G>A NP_001289619.1:n.*107G>A
NM_001302691.1:c.*107G>A NP_001289620.1:n.*107G>A
NM_000041.4:c.*107G>A MANE Select NP_000032.1:n.*107G>A
NM_001302688.2:c.*107G>A NP_001289617.1:n.*107G>A
NM_001302689.2:c.*107G>A NP_001289618.1:n.*107G>A
NM_001302691.2:c.*107G>A NP_001289620.1:n.*107G>A
NM_001302690.2:c.*107G>A NP_001289619.1:n.*107G>A
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