Canonical Allele Identifier: CA507947851

Gene: APOE

Linked Data

• dbSNP Id: rs1400937628
• gnomAD v2: 19-45412351-G-A
• gnomAD v4: 19-44909094-G-A
• MyVariant Identifiers: chr19:g.45412351G>A (hg19) ; chr19:g.44909094G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44909094G>A , CM000681.2:g.44909094G>A	GRCh38
NC_000019.9:g.45412351G>A , CM000681.1:g.45412351G>A	GRCh37
NC_000019.8:g.50104191G>A	NCBI36
NG_007084.2:g.8313G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000252486.9:c.798G>A MANE Select	ENSP00000252486.3:p.Gln266=
ENST00000252486.8:c.798G>A	ENSP00000252486.3:p.Gln266=
NM_000041.3:c.798G>A	NP_000032.1:p.Gln266=
NM_001302688.1:c.876G>A	NP_001289617.1:p.Gln292=
NM_001302689.1:c.798G>A	NP_001289618.1:p.Gln266=
NM_001302690.1:c.798G>A	NP_001289619.1:p.Gln266=
NM_001302691.1:c.798G>A	NP_001289620.1:p.Gln266=
NM_000041.4:c.798G>A MANE Select	NP_000032.1:p.Gln266=
NM_001302688.2:c.876G>A	NP_001289617.1:p.Gln292=
NM_001302689.2:c.798G>A	NP_001289618.1:p.Gln266=
NM_001302691.2:c.798G>A	NP_001289620.1:p.Gln266=
NM_001302690.2:c.798G>A	NP_001289619.1:p.Gln266=