Canonical Allele Identifier: CA2839871203
Gene: APOH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66240235A>C , CM000679.2:g.66240235A>C GRCh38
NC_000017.10:g.64236353A>C , CM000679.1:g.64236353A>C GRCh37
NC_000017.9:g.61666815A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000577982.1:c.-43-10813T>G ENSP00000464301.1:n.-43-10813T>G