Canonical Allele Identifier: CA406304523

Gene: APOE

Linked Data

• gnomAD v4: 19-44908954-C-A
• MyVariant Identifiers: chr19:g.45412211C>A (hg19) ; chr19:g.44908954C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44908954C>A , CM000681.2:g.44908954C>A	GRCh38
NC_000019.9:g.45412211C>A , CM000681.1:g.45412211C>A	GRCh37
NC_000019.8:g.50104051C>A	NCBI36
NG_007084.2:g.8173C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252486.9:c.658C>A MANE Select	ENSP00000252486.3:p.Pro220Thr
ENST00000252486.8:c.658C>A	ENSP00000252486.3:p.Pro220Thr
ENST00000425718.1:c.658C>A
ENST00000434152.5:c.736C>A	ENSP00000413653.2:p.Pro246Thr
NM_000041.3:c.658C>A	NP_000032.1:p.Pro220Thr
NM_001302688.1:c.736C>A	NP_001289617.1:p.Pro246Thr
NM_001302689.1:c.658C>A	NP_001289618.1:p.Pro220Thr
NM_001302690.1:c.658C>A	NP_001289619.1:p.Pro220Thr
NM_001302691.1:c.658C>A	NP_001289620.1:p.Pro220Thr
NM_000041.4:c.658C>A MANE Select	NP_000032.1:p.Pro220Thr
NM_001302688.2:c.736C>A	NP_001289617.1:p.Pro246Thr
NM_001302689.2:c.658C>A	NP_001289618.1:p.Pro220Thr
NM_001302691.2:c.658C>A	NP_001289620.1:p.Pro220Thr
NM_001302690.2:c.658C>A	NP_001289619.1:p.Pro220Thr