Canonical Allele Identifier: CA308886437

Gene: APOE

Linked Data

• dbSNP Id: rs909632766
• gnomAD v3: 19-44909391-G-A
• gnomAD v4: 19-44909391-G-A
• MyVariant Identifiers: chr19:g.45412648G>A (hg19) ; chr19:g.44909391G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44909391G>A , CM000681.2:g.44909391G>A	GRCh38
NC_000019.9:g.45412648G>A , CM000681.1:g.45412648G>A	GRCh37
NC_000019.8:g.50104488G>A	NCBI36
NG_007084.2:g.8610G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252486.9:c.*141G>A MANE Select	ENSP00000252486.3:n.*141G>A
ENST00000252486.8:c.*141G>A	ENSP00000252486.3:n.*141G>A
NM_000041.3:c.*141G>A	NP_000032.1:n.*141G>A
NM_001302688.1:c.*141G>A	NP_001289617.1:n.*141G>A
NM_001302689.1:c.*141G>A	NP_001289618.1:n.*141G>A
NM_001302690.1:c.*141G>A	NP_001289619.1:n.*141G>A
NM_001302691.1:c.*141G>A	NP_001289620.1:n.*141G>A
NM_000041.4:c.*141G>A MANE Select	NP_000032.1:n.*141G>A
NM_001302688.2:c.*141G>A	NP_001289617.1:n.*141G>A
NM_001302689.2:c.*141G>A	NP_001289618.1:n.*141G>A
NM_001302691.2:c.*141G>A	NP_001289620.1:n.*141G>A
NM_001302690.2:c.*141G>A	NP_001289619.1:n.*141G>A