Canonical Allele Identifier: CA2271197033
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs2073512831

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66240175G>A , CM000679.2:g.66240175G>A GRCh38
NC_000017.10:g.64236293G>A , CM000679.1:g.64236293G>A GRCh37
NC_000017.9:g.61666755G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000577982.1:c.-43-10753C>T ENSP00000464301.1:n.-43-10753C>T