Canonical Allele Identifier: CA406302397

Gene: APOE

Linked Data

• gnomAD v4: 19-44907775-T-C
• MyVariant Identifiers: chr19:g.45411032T>C (hg19) ; chr19:g.44907775T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44907775T>C , CM000681.2:g.44907775T>C	GRCh38
NC_000019.9:g.45411032T>C , CM000681.1:g.45411032T>C	GRCh37
NC_000019.8:g.50102872T>C	NCBI36
NG_007084.2:g.6994T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252486.9:c.59T>C MANE Select	ENSP00000252486.3:p.Val20Ala
ENST00000252486.8:c.59T>C	ENSP00000252486.3:p.Val20Ala
ENST00000425718.1:c.59T>C	ENSP00000410423.1:p.Val20Ala
ENST00000434152.5:c.137T>C	ENSP00000413653.2:p.Val46Ala
ENST00000446996.5:c.59T>C	ENSP00000413135.1:p.Val20Ala
NM_000041.3:c.59T>C	NP_000032.1:p.Val20Ala
NM_001302688.1:c.137T>C	NP_001289617.1:p.Val46Ala
NM_001302689.1:c.59T>C	NP_001289618.1:p.Val20Ala
NM_001302690.1:c.59T>C	NP_001289619.1:p.Val20Ala
NM_001302691.1:c.59T>C	NP_001289620.1:p.Val20Ala
NM_000041.4:c.59T>C MANE Select	NP_000032.1:p.Val20Ala
NM_001302688.2:c.137T>C	NP_001289617.1:p.Val46Ala
NM_001302689.2:c.59T>C	NP_001289618.1:p.Val20Ala
NM_001302691.2:c.59T>C	NP_001289620.1:p.Val20Ala
NM_001302690.2:c.59T>C	NP_001289619.1:p.Val20Ala