Canonical Allele Identifier: CA2338168222
Gene: APOE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44909354G= , CM000681.2:g.44909354G= GRCh38
NC_000019.9:g.45412611G= , CM000681.1:g.45412611G= GRCh37
NC_000019.8:g.50104451G= NCBI36
NG_007084.2:g.8573G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252486.9:c.*104G= MANE Select ENSP00000252486.3:n.*104G=
ENST00000252486.8:c.*104G= ENSP00000252486.3:n.*104G=
NM_000041.3:c.*104G= NP_000032.1:n.*104G=
NM_001302688.1:c.*104G= NP_001289617.1:n.*104G=
NM_001302689.1:c.*104G= NP_001289618.1:n.*104G=
NM_001302690.1:c.*104G= NP_001289619.1:n.*104G=
NM_001302691.1:c.*104G= NP_001289620.1:n.*104G=
NM_000041.4:c.*104G= MANE Select NP_000032.1:n.*104G=
NM_001302688.2:c.*104G= NP_001289617.1:n.*104G=
NM_001302689.2:c.*104G= NP_001289618.1:n.*104G=
NM_001302691.2:c.*104G= NP_001289620.1:n.*104G=
NM_001302690.2:c.*104G= NP_001289619.1:n.*104G=