Canonical Allele Identifier: CA2271197032
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs2073512818

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66240176del , CM000679.2:g.66240176del GRCh38
NC_000017.10:g.64236294del , CM000679.1:g.64236294del GRCh37
NC_000017.9:g.61666756del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000577982.1:c.-43-10752del ENSP00000464301.1:n.-43-10752del