Canonical Allele Identifier: CA633314199

Gene: APOE

Linked Data

• dbSNP Id: rs1033095226
• gnomAD v2: 19-45409078-G-C
• gnomAD v4: 19-44905821-G-C
• MyVariant Identifiers: chr19:g.45409078G>C (hg19) ; chr19:g.44905821G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44905821G>C , CM000681.2:g.44905821G>C	GRCh38
NC_000019.9:g.45409078G>C , CM000681.1:g.45409078G>C	GRCh37
NC_000019.8:g.50100918G>C	NCBI36
NG_007084.2:g.5040G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252486.9:c.-44G>C MANE Select	ENSP00000252486.3:n.-44G>C
ENST00000252486.8:c.-44G>C	ENSP00000252486.3:n.-44G>C
ENST00000434152.5:c.-48G>C	ENSP00000413653.2:n.-48G>C
ENST00000446996.5:c.-59G>C	ENSP00000413135.1:n.-59G>C
ENST00000485628.2:n.26G>C
NM_000041.3:c.-44G>C	NP_000032.1:n.-44G>C
NM_001302688.1:c.-48G>C	NP_001289617.1:n.-48G>C
NM_001302691.1:c.-59G>C	NP_001289620.1:n.-59G>C
NM_000041.4:c.-44G>C MANE Select	NP_000032.1:n.-44G>C
NM_001302688.2:c.-48G>C	NP_001289617.1:n.-48G>C
NM_001302691.2:c.-59G>C	NP_001289620.1:n.-59G>C