Canonical Allele Identifier: CA2338168228
Gene: APOE HGNC NCBI

Linked Data

dbSNP Id: rs1969894186
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44909369A>C , CM000681.2:g.44909369A>C GRCh38
NC_000019.9:g.45412626A>C , CM000681.1:g.45412626A>C GRCh37
NC_000019.8:g.50104466A>C NCBI36
NG_007084.2:g.8588A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000252486.9:c.*119A>C MANE Select ENSP00000252486.3:n.*119A>C
ENST00000252486.8:c.*119A>C ENSP00000252486.3:n.*119A>C
NM_000041.3:c.*119A>C NP_000032.1:n.*119A>C
NM_001302688.1:c.*119A>C NP_001289617.1:n.*119A>C
NM_001302689.1:c.*119A>C NP_001289618.1:n.*119A>C
NM_001302690.1:c.*119A>C NP_001289619.1:n.*119A>C
NM_001302691.1:c.*119A>C NP_001289620.1:n.*119A>C
NM_000041.4:c.*119A>C MANE Select NP_000032.1:n.*119A>C
NM_001302688.2:c.*119A>C NP_001289617.1:n.*119A>C
NM_001302689.2:c.*119A>C NP_001289618.1:n.*119A>C
NM_001302691.2:c.*119A>C NP_001289620.1:n.*119A>C
NM_001302690.2:c.*119A>C NP_001289619.1:n.*119A>C
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