Canonical Allele Identifier: CA633314235

Gene: APOE

Linked Data

• dbSNP Id: rs1194835329
• gnomAD v2: 19-45409186-C-A
• gnomAD v4: 19-44905929-C-A
• MyVariant Identifiers: chr19:g.45409186C>A (hg19) ; chr19:g.44905929C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44905929C>A , CM000681.2:g.44905929C>A	GRCh38
NC_000019.9:g.45409186C>A , CM000681.1:g.45409186C>A	GRCh37
NC_000019.8:g.50101026C>A	NCBI36
NG_007084.2:g.5148C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252486.9:c.-24+88C>A MANE Select	ENSP00000252486.3:n.-24+88C>A
ENST00000252486.8:c.-24+88C>A	ENSP00000252486.3:n.-24+88C>A
ENST00000434152.5:c.55+6C>A	ENSP00000413653.2:n.55+6C>A
ENST00000446996.5:c.-39+88C>A	ENSP00000413135.1:n.-39+88C>A
ENST00000485628.2:n.46+88C>A
NM_000041.3:c.-24+88C>A	NP_000032.1:n.-24+88C>A
NM_001302688.1:c.55+6C>A	NP_001289617.1:n.55+6C>A
NM_001302691.1:c.-39+88C>A	NP_001289620.1:n.-39+88C>A
NM_000041.4:c.-24+88C>A MANE Select	NP_000032.1:n.-24+88C>A
NM_001302688.2:c.55+6C>A	NP_001289617.1:n.55+6C>A
NM_001302691.2:c.-39+88C>A	NP_001289620.1:n.-39+88C>A