Canonical Allele Identifier: CA2271197603
Gene: APOH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66240058_66240061delinsAAAG , CM000679.2:g.66240058_66240061delinsAAAG GRCh38
NC_000017.10:g.64236176_64236179delinsAAAG , CM000679.1:g.64236176_64236179delinsAAAG GRCh37
NC_000017.9:g.61666638_61666641delinsAAAG NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000577982.1:c.-43-10639_-43-10636delinsCTTT ENSP00000464301.1:n.-43-10639_-43-10636de...