Canonical Allele Identifier: CA2271197077
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs2073513248

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66240305T>A , CM000679.2:g.66240305T>A GRCh38
NC_000017.10:g.64236423T>A , CM000679.1:g.64236423T>A GRCh37
NC_000017.9:g.61666885T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000577982.1:c.-43-10883A>T ENSP00000464301.1:n.-43-10883A>T