Canonical Allele Identifier: CA774239238

Gene: APOH

Linked Data

• dbSNP Id: rs1196278931
• gnomAD v3: 17-66240010-A-G
• gnomAD v4: 17-66240010-A-G
• MyVariant Identifiers: chr17:g.64236128A>G (hg19) ; chr17:g.66240010A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.66240010A>G , CM000679.2:g.66240010A>G	GRCh38
NC_000017.10:g.64236128A>G , CM000679.1:g.64236128A>G	GRCh37
NC_000017.9:g.61666590A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000577982.1:c.-43-10588T>C	ENSP00000464301.1:n.-43-10588T>C