Canonical Allele Identifier: CA507947600

Gene: APOE

Linked Data

• dbSNP Id: rs1257978352
• gnomAD v2: 19-45412369-C-T
• gnomAD v4: 19-44909112-C-T
• MyVariant Identifiers: chr19:g.45412369C>T (hg19) ; chr19:g.44909112C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44909112C>T , CM000681.2:g.44909112C>T	GRCh38
NC_000019.9:g.45412369C>T , CM000681.1:g.45412369C>T	GRCh37
NC_000019.8:g.50104209C>T	NCBI36
NG_007084.2:g.8331C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252486.9:c.816C>T MANE Select	ENSP00000252486.3:p.Ala272=
ENST00000252486.8:c.816C>T	ENSP00000252486.3:p.Ala272=
NM_000041.3:c.816C>T	NP_000032.1:p.Ala272=
NM_001302688.1:c.894C>T	NP_001289617.1:p.Ala298=
NM_001302689.1:c.816C>T	NP_001289618.1:p.Ala272=
NM_001302690.1:c.816C>T	NP_001289619.1:p.Ala272=
NM_001302691.1:c.816C>T	NP_001289620.1:p.Ala272=
NM_000041.4:c.816C>T MANE Select	NP_000032.1:p.Ala272=
NM_001302688.2:c.894C>T	NP_001289617.1:p.Ala298=
NM_001302689.2:c.816C>T	NP_001289618.1:p.Ala272=
NM_001302691.2:c.816C>T	NP_001289620.1:p.Ala272=
NM_001302690.2:c.816C>T	NP_001289619.1:p.Ala272=