Canonical Allele Identifier: CA2810191532
Gene: APOH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66240056A>G , CM000679.2:g.66240056A>G GRCh38
NC_000017.10:g.64236174A>G , CM000679.1:g.64236174A>G GRCh37
NC_000017.9:g.61666636A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000577982.1:c.-43-10634T>C ENSP00000464301.1:n.-43-10634T>C