Canonical Allele Identifier: CA293120754

Gene: APOH

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.66240125G>C , CM000679.2:g.66240125G>C	GRCh38
NC_000017.10:g.64236243G>C , CM000679.1:g.64236243G>C	GRCh37
NC_000017.9:g.61666705G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000577982.1:c.-43-10703C>G	ENSP00000464301.1:n.-43-10703C>G