Canonical Allele Identifier: CA2271197031
Gene: APOH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66240173_66240174delinsAG , CM000679.2:g.66240173_66240174delinsAG GRCh38
NC_000017.10:g.64236291_64236292delinsAG , CM000679.1:g.64236291_64236292delinsAG GRCh37
NC_000017.9:g.61666753_61666754delinsAG NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000577982.1:c.-43-10752_-43-10751delinsCT ENSP00000464301.1:n.-43-10752_-43-10751de...