Canonical Allele Identifier: CA293120764
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs538270133

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66240173A>C , CM000679.2:g.66240173A>C GRCh38
NC_000017.10:g.64236291A>C , CM000679.1:g.64236291A>C GRCh37
NC_000017.9:g.61666753A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000577982.1:c.-43-10751T>G ENSP00000464301.1:n.-43-10751T>G