Canonical Allele Identifier: CA2338168220
Gene: APOE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44909351G= , CM000681.2:g.44909351G= GRCh38
NC_000019.9:g.45412608G= , CM000681.1:g.45412608G= GRCh37
NC_000019.8:g.50104448G= NCBI36
NG_007084.2:g.8570G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252486.9:c.*101G= MANE Select ENSP00000252486.3:n.*101G=
ENST00000252486.8:c.*101G= ENSP00000252486.3:n.*101G=
NM_000041.3:c.*101G= NP_000032.1:n.*101G=
NM_001302688.1:c.*101G= NP_001289617.1:n.*101G=
NM_001302689.1:c.*101G= NP_001289618.1:n.*101G=
NM_001302690.1:c.*101G= NP_001289619.1:n.*101G=
NM_001302691.1:c.*101G= NP_001289620.1:n.*101G=
NM_000041.4:c.*101G= MANE Select NP_000032.1:n.*101G=
NM_001302688.2:c.*101G= NP_001289617.1:n.*101G=
NM_001302689.2:c.*101G= NP_001289618.1:n.*101G=
NM_001302691.2:c.*101G= NP_001289620.1:n.*101G=
NM_001302690.2:c.*101G= NP_001289619.1:n.*101G=