Canonical Allele Identifier: CA293120798
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs971159690

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66240312G>A , CM000679.2:g.66240312G>A GRCh38
NC_000017.10:g.64236430G>A , CM000679.1:g.64236430G>A GRCh37
NC_000017.9:g.61666892G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000577982.1:c.-43-10890C>T ENSP00000464301.1:n.-43-10890C>T