Canonical Allele Identifier: CA2847531131
Gene: APOH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66240200_66240207del , CM000679.2:g.66240200_66240207del GRCh38
NC_000017.10:g.64236318_64236325del , CM000679.1:g.64236318_64236325del GRCh37
NC_000017.9:g.61666780_61666787del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000577982.1:c.-43-10785_-43-10778del ENSP00000464301.1:n.-43-10785_-43-10778del