Canonical Allele Identifier: CA2810191542
Gene: APOH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66240257G>T , CM000679.2:g.66240257G>T GRCh38
NC_000017.10:g.64236375G>T , CM000679.1:g.64236375G>T GRCh37
NC_000017.9:g.61666837G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000577982.1:c.-43-10835C>A ENSP00000464301.1:n.-43-10835C>A