Canonical Allele Identifier: CA2271197048
Gene: APOH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66240221T= , CM000679.2:g.66240221T= GRCh38
NC_000017.10:g.64236339T= , CM000679.1:g.64236339T= GRCh37
NC_000017.9:g.61666801T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000577982.1:c.-43-10799A= ENSP00000464301.1:n.-43-10799A=