Canonical Allele Identifier: CA293120747

Gene: APOH

Linked Data

• dbSNP Id: rs891744666
• MyVariant Identifiers: chr17:g.64236196G>T (hg19) ; chr17:g.66240078G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.66240078G>T , CM000679.2:g.66240078G>T	GRCh38
NC_000017.10:g.64236196G>T , CM000679.1:g.64236196G>T	GRCh37
NC_000017.9:g.61666658G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000577982.1:c.-43-10656C>A	ENSP00000464301.1:n.-43-10656C>A