Canonical Allele Identifier: CA9505964

Gene: APOE

Linked Data

• dbSNP Id: rs774067024
• ExAC: 19:45411000 G / A
• gnomAD v2: 19-45411000-G-A
• gnomAD v4: 19-44907743-G-A
• MyVariant Identifiers: chr19:g.45411000G>A (hg19) ; chr19:g.44907743G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44907743G>A , CM000681.2:g.44907743G>A	GRCh38
NC_000019.9:g.45411000G>A , CM000681.1:g.45411000G>A	GRCh37
NC_000019.8:g.50102840G>A	NCBI36
NG_007084.2:g.6962G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000252486.9:c.44-17G>A MANE Select	ENSP00000252486.3:n.44-17G>A
ENST00000252486.8:c.44-17G>A	ENSP00000252486.3:n.44-17G>A
ENST00000425718.1:c.44-17G>A	ENSP00000410423.1:n.44-17G>A
ENST00000434152.5:c.122-17G>A	ENSP00000413653.2:n.122-17G>A
ENST00000446996.5:c.44-17G>A	ENSP00000413135.1:n.44-17G>A
NM_000041.3:c.44-17G>A	NP_000032.1:n.44-17G>A
NM_001302688.1:c.122-17G>A	NP_001289617.1:n.122-17G>A
NM_001302689.1:c.44-17G>A	NP_001289618.1:n.44-17G>A
NM_001302690.1:c.44-17G>A	NP_001289619.1:n.44-17G>A
NM_001302691.1:c.44-17G>A	NP_001289620.1:n.44-17G>A
NM_000041.4:c.44-17G>A MANE Select	NP_000032.1:n.44-17G>A
NM_001302688.2:c.122-17G>A	NP_001289617.1:n.122-17G>A
NM_001302689.2:c.44-17G>A	NP_001289618.1:n.44-17G>A
NM_001302691.2:c.44-17G>A	NP_001289620.1:n.44-17G>A
NM_001302690.2:c.44-17G>A	NP_001289619.1:n.44-17G>A