Canonical Allele Identifier: CA2338167661
Gene: APOE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44908733A= , CM000681.2:g.44908733A= GRCh38
NC_000019.9:g.45411990A= , CM000681.1:g.45411990A= GRCh37
NC_000019.8:g.50103830A= NCBI36
NG_007084.2:g.7952A=

Transcript Alleles

HGVS Amino-acid change
ENST00000252486.9:c.437A= MANE Select ENSP00000252486.3:p.Gln146=
ENST00000252486.8:c.437A= ENSP00000252486.3:p.Gln146=
ENST00000425718.1:c.437A= ENSP00000410423.1:p.Gln146=
ENST00000434152.5:c.515A= ENSP00000413653.2:p.Gln172=
ENST00000446996.5:c.437A= ENSP00000413135.1:p.Gln146=
NM_000041.3:c.437A= NP_000032.1:p.Gln146=
NM_001302688.1:c.515A= NP_001289617.1:p.Gln172=
NM_001302689.1:c.437A= NP_001289618.1:p.Gln146=
NM_001302690.1:c.437A= NP_001289619.1:p.Gln146=
NM_001302691.1:c.437A= NP_001289620.1:p.Gln146=
NM_000041.4:c.437A= MANE Select NP_000032.1:p.Gln146=
NM_001302688.2:c.515A= NP_001289617.1:p.Gln172=
NM_001302689.2:c.437A= NP_001289618.1:p.Gln146=
NM_001302691.2:c.437A= NP_001289620.1:p.Gln146=
NM_001302690.2:c.437A= NP_001289619.1:p.Gln146=