Canonical Allele Identifier: CA882661603

Gene: APOE

Linked Data

• dbSNP Id: rs1332689064
• gnomAD v3: 19-44905831-C-T
• gnomAD v4: 19-44905831-C-T
• MyVariant Identifiers: chr19:g.45409088C>T (hg19) ; chr19:g.44905831C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44905831C>T , CM000681.2:g.44905831C>T	GRCh38
NC_000019.9:g.45409088C>T , CM000681.1:g.45409088C>T	GRCh37
NC_000019.8:g.50100928C>T	NCBI36
NG_007084.2:g.5050C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252486.9:c.-34C>T MANE Select	ENSP00000252486.3:n.-34C>T
ENST00000252486.8:c.-34C>T	ENSP00000252486.3:n.-34C>T
ENST00000434152.5:c.-38C>T	ENSP00000413653.2:n.-38C>T
ENST00000446996.5:c.-49C>T	ENSP00000413135.1:n.-49C>T
ENST00000485628.2:n.36C>T
NM_000041.3:c.-34C>T	NP_000032.1:n.-34C>T
NM_001302688.1:c.-38C>T	NP_001289617.1:n.-38C>T
NM_001302691.1:c.-49C>T	NP_001289620.1:n.-49C>T
NM_000041.4:c.-34C>T MANE Select	NP_000032.1:n.-34C>T
NM_001302688.2:c.-38C>T	NP_001289617.1:n.-38C>T
NM_001302691.2:c.-49C>T	NP_001289620.1:n.-49C>T