Canonical Allele Identifier: CA985616773
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs2073512441

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66240062_66240066del , CM000679.2:g.66240062_66240066del GRCh38
NC_000017.10:g.64236180_64236184del , CM000679.1:g.64236180_64236184del GRCh37
NC_000017.9:g.61666642_61666646del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000577982.1:c.-43-10644_-43-10640del ENSP00000464301.1:n.-43-10644_-43-10640de...