Canonical Allele Identifier: CA996247967
Gene: APOE HGNC NCBI

Linked Data

dbSNP Id: rs1969894600
gnomAD v3: 19-44909395-C-T
gnomAD v4: 19-44909395-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44909395C>T , CM000681.2:g.44909395C>T GRCh38
NC_000019.9:g.45412652C>T , CM000681.1:g.45412652C>T GRCh37
NC_000019.8:g.50104492C>T NCBI36
NG_007084.2:g.8614C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000041.3:c.*145C>T NP_000032.1:n.*145C>T
NM_001302688.1:c.*145C>T NP_001289617.1:n.*145C>T
NM_001302689.1:c.*145C>T NP_001289618.1:n.*145C>T
NM_001302690.1:c.*145C>T NP_001289619.1:n.*145C>T
NM_001302691.1:c.*145C>T NP_001289620.1:n.*145C>T
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