Canonical Allele Identifier: CA626914198
Gene: APOH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66240174_66240175insT , CM000679.2:g.66240174_66240175insT GRCh38
NC_000017.10:g.64236292_64236293insT , CM000679.1:g.64236292_64236293insT GRCh37
NC_000017.9:g.61666754_61666755insT NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000577982.1:c.-43-10753_-43-10752insA ENSP00000464301.1:n.-43-10753_-43-10752in...