Canonical Allele Identifier: CA2271197608
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs2073512450

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66240067_66240069del , CM000679.2:g.66240067_66240069del GRCh38
NC_000017.10:g.64236185_64236187del , CM000679.1:g.64236185_64236187del GRCh37
NC_000017.9:g.61666647_61666649del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000577982.1:c.-43-10647_-43-10645del ENSP00000464301.1:n.-43-10647_-43-10645de...