Canonical Allele Identifier: CA996247106

Gene: APOE

Linked Data

• dbSNP Id: rs1969834079
• gnomAD v3: 19-44907755-C-T
• gnomAD v4: 19-44907755-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44907755C>T , CM000681.2:g.44907755C>T	GRCh38
NC_000019.9:g.45411012C>T , CM000681.1:g.45411012C>T	GRCh37
NC_000019.8:g.50102852C>T	NCBI36
NG_007084.2:g.6974C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000252486.9:c.44-5C>T MANE Select	ENSP00000252486.3:n.44-5C>T
ENST00000252486.8:c.44-5C>T	ENSP00000252486.3:n.44-5C>T
ENST00000425718.1:c.44-5C>T	ENSP00000410423.1:n.44-5C>T
ENST00000434152.5:c.122-5C>T	ENSP00000413653.2:n.122-5C>T
ENST00000446996.5:c.44-5C>T	ENSP00000413135.1:n.44-5C>T
NM_000041.3:c.44-5C>T	NP_000032.1:n.44-5C>T
NM_001302688.1:c.122-5C>T	NP_001289617.1:n.122-5C>T
NM_001302689.1:c.44-5C>T	NP_001289618.1:n.44-5C>T
NM_001302690.1:c.44-5C>T	NP_001289619.1:n.44-5C>T
NM_001302691.1:c.44-5C>T	NP_001289620.1:n.44-5C>T
NM_000041.4:c.44-5C>T MANE Select	NP_000032.1:n.44-5C>T
NM_001302688.2:c.122-5C>T	NP_001289617.1:n.122-5C>T
NM_001302689.2:c.44-5C>T	NP_001289618.1:n.44-5C>T
NM_001302691.2:c.44-5C>T	NP_001289620.1:n.44-5C>T
NM_001302690.2:c.44-5C>T	NP_001289619.1:n.44-5C>T