Canonical Allele Identifier: CA406301498
Gene: APOE HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44905920C>T , CM000681.2:g.44905920C>T GRCh38
NC_000019.9:g.45409177C>T , CM000681.1:g.45409177C>T GRCh37
NC_000019.8:g.50101017C>T NCBI36
NG_007084.2:g.5139C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000252486.9:c.-24+79C>T MANE Select ENSP00000252486.3:n.-24+79C>T
ENST00000252486.8:c.-24+79C>T ENSP00000252486.3:n.-24+79C>T
ENST00000434152.5:c.52C>T ENSP00000413653.2:p.Pro18Ser
ENST00000446996.5:c.-39+79C>T ENSP00000413135.1:n.-39+79C>T
ENST00000485628.2:n.46+79C>T
NM_000041.3:c.-24+79C>T NP_000032.1:n.-24+79C>T
NM_001302688.1:c.52C>T NP_001289617.1:p.Pro18Ser
NM_001302691.1:c.-39+79C>T NP_001289620.1:n.-39+79C>T
NM_000041.4:c.-24+79C>T MANE Select NP_000032.1:n.-24+79C>T
NM_001302688.2:c.52C>T NP_001289617.1:p.Pro18Ser
NM_001302691.2:c.-39+79C>T NP_001289620.1:n.-39+79C>T