Canonical Allele Identifier: CA2271197015
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs2073512724

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66240144G>A , CM000679.2:g.66240144G>A GRCh38
NC_000017.10:g.64236262G>A , CM000679.1:g.64236262G>A GRCh37
NC_000017.9:g.61666724G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000577982.1:c.-43-10722C>T ENSP00000464301.1:n.-43-10722C>T