Canonical Allele Identifier: CA511291339
Gene: MIR646HG HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.58895842C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.60320784C>G , CM000682.2:g.60320784C>G GRCh38
NC_000020.10:g.58895842C>G , CM000682.1:g.58895842C>G GRCh37
NC_000020.9:g.58329237C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046099.1:n.571C>G
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