Canonical Allele Identifier: CA406303654

Gene: APOE

Linked Data

• dbSNP Id: rs1434287349
• gnomAD v2: 19-45411809-A-G
• gnomAD v4: 19-44908552-A-G
• MyVariant Identifiers: chr19:g.45411809A>G (hg19) ; chr19:g.44908552A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44908552A>G , CM000681.2:g.44908552A>G	GRCh38
NC_000019.9:g.45411809A>G , CM000681.1:g.45411809A>G	GRCh37
NC_000019.8:g.50103649A>G	NCBI36
NG_007084.2:g.7771A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252486.9:c.256A>G MANE Select	ENSP00000252486.3:p.Met86Val
ENST00000252486.8:c.256A>G	ENSP00000252486.3:p.Met86Val
ENST00000425718.1:c.256A>G	ENSP00000410423.1:p.Met86Val
ENST00000434152.5:c.334A>G	ENSP00000413653.2:p.Met112Val
ENST00000446996.5:c.256A>G	ENSP00000413135.1:p.Met86Val
NM_000041.3:c.256A>G	NP_000032.1:p.Met86Val
NM_001302688.1:c.334A>G	NP_001289617.1:p.Met112Val
NM_001302689.1:c.256A>G	NP_001289618.1:p.Met86Val
NM_001302690.1:c.256A>G	NP_001289619.1:p.Met86Val
NM_001302691.1:c.256A>G	NP_001289620.1:p.Met86Val
NM_000041.4:c.256A>G MANE Select	NP_000032.1:p.Met86Val
NM_001302688.2:c.334A>G	NP_001289617.1:p.Met112Val
NM_001302689.2:c.256A>G	NP_001289618.1:p.Met86Val
NM_001302691.2:c.256A>G	NP_001289620.1:p.Met86Val
NM_001302690.2:c.256A>G	NP_001289619.1:p.Met86Val