Canonical Allele Identifier: CA633314198

Gene: APOE

Linked Data

• dbSNP Id: rs1157180379
• gnomAD v2: 19-45409073-T-G
• gnomAD v4: 19-44905816-T-G
• MyVariant Identifiers: chr19:g.45409073T>G (hg19) ; chr19:g.44905816T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44905816T>G , CM000681.2:g.44905816T>G	GRCh38
NC_000019.9:g.45409073T>G , CM000681.1:g.45409073T>G	GRCh37
NC_000019.8:g.50100913T>G	NCBI36
NG_007084.2:g.5035T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252486.9:c.-49T>G MANE Select	ENSP00000252486.3:n.-49T>G
ENST00000252486.8:c.-49T>G	ENSP00000252486.3:n.-49T>G
ENST00000434152.5:c.-53T>G	ENSP00000413653.2:n.-53T>G
ENST00000446996.5:c.-64T>G	ENSP00000413135.1:n.-64T>G
ENST00000485628.2:n.21T>G
NM_000041.3:c.-49T>G	NP_000032.1:n.-49T>G
NM_001302688.1:c.-53T>G	NP_001289617.1:n.-53T>G
NM_001302691.1:c.-64T>G	NP_001289620.1:n.-64T>G
NM_000041.4:c.-49T>G MANE Select	NP_000032.1:n.-49T>G
NM_001302688.2:c.-53T>G	NP_001289617.1:n.-53T>G
NM_001302691.2:c.-64T>G	NP_001289620.1:n.-64T>G