Canonical Allele Identifier: CA2271197083
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs2073513292

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66240313G>C , CM000679.2:g.66240313G>C GRCh38
NC_000017.10:g.64236431G>C , CM000679.1:g.64236431G>C GRCh37
NC_000017.9:g.61666893G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000577982.1:c.-43-10891C>G ENSP00000464301.1:n.-43-10891C>G