Canonical Allele Identifier: CA293120734
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs908132134
MyVariant Identifiers: chr17:g.64236146G>A (hg19) chr17:g.66240028G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66240028G>A , CM000679.2:g.66240028G>A GRCh38
NC_000017.10:g.64236146G>A , CM000679.1:g.64236146G>A GRCh37
NC_000017.9:g.61666608G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000577982.1:c.-43-10606C>T ENSP00000464301.1:n.-43-10606C>T
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