Canonical Allele Identifier: CA293120765

Gene: APOH

Linked Data

• dbSNP Id: rs558557841
• gnomAD v2: 17-64236294-G-A
• gnomAD v3: 17-66240176-G-A
• gnomAD v4: 17-66240176-G-A
• MyVariant Identifiers: chr17:g.64236294G>A (hg19) ; chr17:g.66240176G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.66240176G>A , CM000679.2:g.66240176G>A	GRCh38
NC_000017.10:g.64236294G>A , CM000679.1:g.64236294G>A	GRCh37
NC_000017.9:g.61666756G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000577982.1:c.-43-10754C>T	ENSP00000464301.1:n.-43-10754C>T