Canonical Allele Identifier: CA2373187684
Gene: MIR646HG HGNC NCBI

Linked Data

dbSNP Id: rs1981174719
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.60320534C>A , CM000682.2:g.60320534C>A GRCh38
NC_000020.10:g.58895592C>A , CM000682.1:g.58895592C>A GRCh37
NC_000020.9:g.58328987C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046099.1:n.420-99C>A
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Search 100 bp 3'