Canonical Allele Identifier: CA2810191529
Gene: APOH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66240010A>C , CM000679.2:g.66240010A>C GRCh38
NC_000017.10:g.64236128A>C , CM000679.1:g.64236128A>C GRCh37
NC_000017.9:g.61666590A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000577982.1:c.-43-10588T>G ENSP00000464301.1:n.-43-10588T>G