Canonical Allele Identifier: CA2271197315
Gene: APOH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66239682A= , CM000679.2:g.66239682A= GRCh38
NC_000017.10:g.64235800A= , CM000679.1:g.64235800A= GRCh37
NC_000017.9:g.61666262A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000577982.1:c.-43-10260T= ENSP00000464301.1:n.-43-10260T=