Canonical Allele Identifier: CA2810191502
Gene: APOH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66239615C>A , CM000679.2:g.66239615C>A GRCh38
NC_000017.10:g.64235733C>A , CM000679.1:g.64235733C>A GRCh37
NC_000017.9:g.61666195C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000577982.1:c.-43-10193G>T ENSP00000464301.1:n.-43-10193G>T
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