Canonical Allele Identifier: CA2585715571

Gene: APOE

Linked Data

• gnomAD v4: 19-44909351-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44909351G>C , CM000681.2:g.44909351G>C	GRCh38
NC_000019.9:g.45412608G>C , CM000681.1:g.45412608G>C	GRCh37
NC_000019.8:g.50104448G>C	NCBI36
NG_007084.2:g.8570G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252486.9:c.*101G>C MANE Select	ENSP00000252486.3:n.*101G>C
ENST00000252486.8:c.*101G>C	ENSP00000252486.3:n.*101G>C
NM_000041.3:c.*101G>C	NP_000032.1:n.*101G>C
NM_001302688.1:c.*101G>C	NP_001289617.1:n.*101G>C
NM_001302689.1:c.*101G>C	NP_001289618.1:n.*101G>C
NM_001302690.1:c.*101G>C	NP_001289619.1:n.*101G>C
NM_001302691.1:c.*101G>C	NP_001289620.1:n.*101G>C
NM_000041.4:c.*101G>C MANE Select	NP_000032.1:n.*101G>C
NM_001302688.2:c.*101G>C	NP_001289617.1:n.*101G>C
NM_001302689.2:c.*101G>C	NP_001289618.1:n.*101G>C
NM_001302691.2:c.*101G>C	NP_001289620.1:n.*101G>C
NM_001302690.2:c.*101G>C	NP_001289619.1:n.*101G>C