Canonical Allele Identifier: CA293120778
Gene: APOH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66240233C>T , CM000679.2:g.66240233C>T GRCh38
NC_000017.10:g.64236351C>T , CM000679.1:g.64236351C>T GRCh37
NC_000017.9:g.61666813C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000577982.1:c.-43-10811G>A ENSP00000464301.1:n.-43-10811G>A