Canonical Allele Identifier: CA293120767

Gene: APOH

Linked Data

• dbSNP Id: rs569001876
• gnomAD v2: 17-64236301-G-T
• gnomAD v3: 17-66240183-G-T
• gnomAD v4: 17-66240183-G-T
• MyVariant Identifiers: chr17:g.64236301G>T (hg19) ; chr17:g.66240183G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.66240183G>T , CM000679.2:g.66240183G>T	GRCh38
NC_000017.10:g.64236301G>T , CM000679.1:g.64236301G>T	GRCh37
NC_000017.9:g.61666763G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000577982.1:c.-43-10761C>A	ENSP00000464301.1:n.-43-10761C>A