Canonical Allele Identifier: CA2271197289
Gene: APOH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66239659G= , CM000679.2:g.66239659G= GRCh38
NC_000017.10:g.64235777G= , CM000679.1:g.64235777G= GRCh37
NC_000017.9:g.61666239G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000577982.1:c.-43-10237C= ENSP00000464301.1:n.-43-10237C=