Canonical Allele Identifier: CA2338167912
Gene: APOE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44908836C= , CM000681.2:g.44908836C= GRCh38
NC_000019.9:g.45412093C= , CM000681.1:g.45412093C= GRCh37
NC_000019.8:g.50103933C= NCBI36
NG_007084.2:g.8055C=

Transcript Alleles

HGVS Amino-acid change
ENST00000252486.9:c.540C= MANE Select ENSP00000252486.3:p.Tyr180=
ENST00000252486.8:c.540C= ENSP00000252486.3:p.Tyr180=
ENST00000425718.1:c.540C= ENSP00000410423.1:p.Tyr180=
ENST00000434152.5:c.618C= ENSP00000413653.2:p.Tyr206=
ENST00000446996.5:c.540C= ENSP00000413135.1:p.Tyr180=
NM_000041.3:c.540C= NP_000032.1:p.Tyr180=
NM_001302688.1:c.618C= NP_001289617.1:p.Tyr206=
NM_001302689.1:c.540C= NP_001289618.1:p.Tyr180=
NM_001302690.1:c.540C= NP_001289619.1:p.Tyr180=
NM_001302691.1:c.540C= NP_001289620.1:p.Tyr180=
NM_000041.4:c.540C= MANE Select NP_000032.1:p.Tyr180=
NM_001302688.2:c.618C= NP_001289617.1:p.Tyr206=
NM_001302689.2:c.540C= NP_001289618.1:p.Tyr180=
NM_001302691.2:c.540C= NP_001289620.1:p.Tyr180=
NM_001302690.2:c.540C= NP_001289619.1:p.Tyr180=