Canonical Allele Identifier: CA317000042
Gene: MIR646HG HGNC NCBI

Linked Data

dbSNP Id: rs898933074
MyVariant Identifiers: chr20:g.58895648G>T (hg19) chr20:g.60320590G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.60320590G>T , CM000682.2:g.60320590G>T GRCh38
NC_000020.10:g.58895648G>T , CM000682.1:g.58895648G>T GRCh37
NC_000020.9:g.58329043G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046099.1:n.420-43G>T
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