Canonical Allele Identifier: CA774239208

Gene: APOH

Linked Data

• dbSNP Id: rs1364532127
• gnomAD v3: 17-66239969-C-A
• gnomAD v4: 17-66239969-C-A
• MyVariant Identifiers: chr17:g.64236087C>A (hg19) ; chr17:g.66239969C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.66239969C>A , CM000679.2:g.66239969C>A	GRCh38
NC_000017.10:g.64236087C>A , CM000679.1:g.64236087C>A	GRCh37
NC_000017.9:g.61666549C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000577982.1:c.-43-10547G>T	ENSP00000464301.1:n.-43-10547G>T