Canonical Allele Identifier: CA511291451
Gene: MIR646HG HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.58895882C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.60320824C>A , CM000682.2:g.60320824C>A GRCh38
NC_000020.10:g.58895882C>A , CM000682.1:g.58895882C>A GRCh37
NC_000020.9:g.58329277C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046099.1:n.611C>A
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