Canonical Allele Identifier: CA317000054
Gene: MIR646HG HGNC NCBI

Linked Data

dbSNP Id: rs1030263891
MyVariant Identifiers: chr20:g.58895797A>G (hg19) chr20:g.60320739A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.60320739A>G , CM000682.2:g.60320739A>G GRCh38
NC_000020.10:g.58895797A>G , CM000682.1:g.58895797A>G GRCh37
NC_000020.9:g.58329192A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046099.1:n.526A>G
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