Canonical Allele Identifier: CA293120754
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs868102592

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66240125G>C , CM000679.2:g.66240125G>C GRCh38
NC_000017.10:g.64236243G>C , CM000679.1:g.64236243G>C GRCh37
NC_000017.9:g.61666705G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000577982.1:c.-43-10703C>G ENSP00000464301.1:n.-43-10703C>G