Canonical Allele Identifier: CA406303902
Gene: APOE HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44908673T>A , CM000681.2:g.44908673T>A GRCh38
NC_000019.9:g.45411930T>A , CM000681.1:g.45411930T>A GRCh37
NC_000019.8:g.50103770T>A NCBI36
NG_007084.2:g.7892T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000252486.9:c.377T>A MANE Select ENSP00000252486.3:p.Met126Lys
ENST00000252486.8:c.377T>A ENSP00000252486.3:p.Met126Lys
ENST00000425718.1:c.377T>A ENSP00000410423.1:p.Met126Lys
ENST00000434152.5:c.455T>A ENSP00000413653.2:p.Met152Lys
ENST00000446996.5:c.377T>A ENSP00000413135.1:p.Met126Lys
NM_000041.3:c.377T>A NP_000032.1:p.Met126Lys
NM_001302688.1:c.455T>A NP_001289617.1:p.Met152Lys
NM_001302689.1:c.377T>A NP_001289618.1:p.Met126Lys
NM_001302690.1:c.377T>A NP_001289619.1:p.Met126Lys
NM_001302691.1:c.377T>A NP_001289620.1:p.Met126Lys
NM_000041.4:c.377T>A MANE Select NP_000032.1:p.Met126Lys
NM_001302688.2:c.455T>A NP_001289617.1:p.Met152Lys
NM_001302689.2:c.377T>A NP_001289618.1:p.Met126Lys
NM_001302691.2:c.377T>A NP_001289620.1:p.Met126Lys
NM_001302690.2:c.377T>A NP_001289619.1:p.Met126Lys