Canonical Allele Identifier: CA406305634

Gene: APOE

Linked Data

• MyVariant Identifiers: chr19:g.45412403G>C (hg19) ; chr19:g.44909146G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44909146G>C , CM000681.2:g.44909146G>C	GRCh38
NC_000019.9:g.45412403G>C , CM000681.1:g.45412403G>C	GRCh37
NC_000019.8:g.50104243G>C	NCBI36
NG_007084.2:g.8365G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000252486.9:c.850G>C MANE Select	ENSP00000252486.3:p.Glu284Gln
ENST00000252486.8:c.850G>C	ENSP00000252486.3:p.Glu284Gln
NM_000041.3:c.850G>C	NP_000032.1:p.Glu284Gln
NM_001302688.1:c.928G>C	NP_001289617.1:p.Glu310Gln
NM_001302689.1:c.850G>C	NP_001289618.1:p.Glu284Gln
NM_001302690.1:c.850G>C	NP_001289619.1:p.Glu284Gln
NM_001302691.1:c.850G>C	NP_001289620.1:p.Glu284Gln
NM_000041.4:c.850G>C MANE Select	NP_000032.1:p.Glu284Gln
NM_001302688.2:c.928G>C	NP_001289617.1:p.Glu310Gln
NM_001302689.2:c.850G>C	NP_001289618.1:p.Glu284Gln
NM_001302691.2:c.850G>C	NP_001289620.1:p.Glu284Gln
NM_001302690.2:c.850G>C	NP_001289619.1:p.Glu284Gln