Canonical Allele Identifier: CA2271197279
Gene: APOH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66239649_66239651delinsTGA , CM000679.2:g.66239649_66239651delinsTGA GRCh38
NC_000017.10:g.64235767_64235769delinsTGA , CM000679.1:g.64235767_64235769delinsTGA GRCh37
NC_000017.9:g.61666229_61666231delinsTGA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000577982.1:c.-43-10229_-43-10227delinsTCA ENSP00000464301.1:n.-43-10229_-43-10227delinsTCA