Canonical Allele Identifier: CA2810191539

Gene: APOH

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.66240231G>T , CM000679.2:g.66240231G>T	GRCh38
NC_000017.10:g.64236349G>T , CM000679.1:g.64236349G>T	GRCh37
NC_000017.9:g.61666811G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000577982.1:c.-43-10809C>A	ENSP00000464301.1:n.-43-10809C>A