Canonical Allele Identifier: CA293120816
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs925715864
COSMIC: COSN7442991
MyVariant Identifiers: chr17:g.64236471G>A (hg19) chr17:g.66240353G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66240353G>A , CM000679.2:g.66240353G>A GRCh38
NC_000017.10:g.64236471G>A , CM000679.1:g.64236471G>A GRCh37
NC_000017.9:g.61666933G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000577982.1:c.-43-10931C>T ENSP00000464301.1:n.-43-10931C>T
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