Canonical Allele Identifier: CA2585713825

Gene: APOE

Linked Data

• gnomAD v4: 19-44905935-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44905935A>C , CM000681.2:g.44905935A>C	GRCh38
NC_000019.9:g.45409192A>C , CM000681.1:g.45409192A>C	GRCh37
NC_000019.8:g.50101032A>C	NCBI36
NG_007084.2:g.5154A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252486.9:c.-24+94A>C MANE Select	ENSP00000252486.3:n.-24+94A>C
ENST00000252486.8:c.-24+94A>C	ENSP00000252486.3:n.-24+94A>C
ENST00000434152.5:c.55+12A>C	ENSP00000413653.2:n.55+12A>C
ENST00000446996.5:c.-39+94A>C	ENSP00000413135.1:n.-39+94A>C
ENST00000485628.2:n.46+94A>C
NM_000041.3:c.-24+94A>C	NP_000032.1:n.-24+94A>C
NM_001302688.1:c.55+12A>C	NP_001289617.1:n.55+12A>C
NM_001302691.1:c.-39+94A>C	NP_001289620.1:n.-39+94A>C
NM_000041.4:c.-24+94A>C MANE Select	NP_000032.1:n.-24+94A>C
NM_001302688.2:c.55+12A>C	NP_001289617.1:n.55+12A>C
NM_001302691.2:c.-39+94A>C	NP_001289620.1:n.-39+94A>C