Canonical Allele Identifier: CA2271197029
Gene: APOH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66240170A= , CM000679.2:g.66240170A= GRCh38
NC_000017.10:g.64236288A= , CM000679.1:g.64236288A= GRCh37
NC_000017.9:g.61666750A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000577982.1:c.-43-10748T= ENSP00000464301.1:n.-43-10748T=