Canonical Allele Identifier: CA882664974

Gene: APOE

Linked Data

• dbSNP Id: rs1246294239
• gnomAD v3: 19-44909377-T-A
• gnomAD v4: 19-44909377-T-A
• MyVariant Identifiers: chr19:g.45412634T>A (hg19) ; chr19:g.44909377T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44909377T>A , CM000681.2:g.44909377T>A	GRCh38
NC_000019.9:g.45412634T>A , CM000681.1:g.45412634T>A	GRCh37
NC_000019.8:g.50104474T>A	NCBI36
NG_007084.2:g.8596T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252486.9:c.*127T>A MANE Select	ENSP00000252486.3:n.*127T>A
ENST00000252486.8:c.*127T>A	ENSP00000252486.3:n.*127T>A
NM_000041.3:c.*127T>A	NP_000032.1:n.*127T>A
NM_001302688.1:c.*127T>A	NP_001289617.1:n.*127T>A
NM_001302689.1:c.*127T>A	NP_001289618.1:n.*127T>A
NM_001302690.1:c.*127T>A	NP_001289619.1:n.*127T>A
NM_001302691.1:c.*127T>A	NP_001289620.1:n.*127T>A
NM_000041.4:c.*127T>A MANE Select	NP_000032.1:n.*127T>A
NM_001302688.2:c.*127T>A	NP_001289617.1:n.*127T>A
NM_001302689.2:c.*127T>A	NP_001289618.1:n.*127T>A
NM_001302691.2:c.*127T>A	NP_001289620.1:n.*127T>A
NM_001302690.2:c.*127T>A	NP_001289619.1:n.*127T>A