Canonical Allele Identifier: CA2521940769
Gene: APOH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66240300T>A , CM000679.2:g.66240300T>A GRCh38
NC_000017.10:g.64236418T>A , CM000679.1:g.64236418T>A GRCh37
NC_000017.9:g.61666880T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000577982.1:c.-43-10878A>T ENSP00000464301.1:n.-43-10878A>T