Canonical Allele Identifier: CA308885733

Gene: APOE

Linked Data

• dbSNP Id: rs868094551
• gnomAD v4: 19-44908768-C-A
• MyVariant Identifiers: chr19:g.45412025C>A (hg19) ; chr19:g.44908768C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44908768C>A , CM000681.2:g.44908768C>A	GRCh38
NC_000019.9:g.45412025C>A , CM000681.1:g.45412025C>A	GRCh37
NC_000019.8:g.50103865C>A	NCBI36
NG_007084.2:g.7987C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000252486.9:c.472C>A MANE Select	ENSP00000252486.3:p.His158Asn
ENST00000252486.8:c.472C>A	ENSP00000252486.3:p.His158Asn
ENST00000425718.1:c.472C>A	ENSP00000410423.1:p.His158Asn
ENST00000434152.5:c.550C>A	ENSP00000413653.2:p.His184Asn
ENST00000446996.5:c.472C>A	ENSP00000413135.1:p.His158Asn
NM_000041.3:c.472C>A	NP_000032.1:p.His158Asn
NM_001302688.1:c.550C>A	NP_001289617.1:p.His184Asn
NM_001302689.1:c.472C>A	NP_001289618.1:p.His158Asn
NM_001302690.1:c.472C>A	NP_001289619.1:p.His158Asn
NM_001302691.1:c.472C>A	NP_001289620.1:p.His158Asn
NM_000041.4:c.472C>A MANE Select	NP_000032.1:p.His158Asn
NM_001302688.2:c.550C>A	NP_001289617.1:p.His184Asn
NM_001302689.2:c.472C>A	NP_001289618.1:p.His158Asn
NM_001302691.2:c.472C>A	NP_001289620.1:p.His158Asn
NM_001302690.2:c.472C>A	NP_001289619.1:p.His158Asn