Canonical Allele Identifier: CA511291406
Gene: MIR646HG HGNC NCBI

Linked Data

dbSNP Id: rs1981183170
gnomAD v4: 20-60320808-C-A
MyVariant Identifiers: chr20:g.58895866C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.60320808C>A , CM000682.2:g.60320808C>A GRCh38
NC_000020.10:g.58895866C>A , CM000682.1:g.58895866C>A GRCh37
NC_000020.9:g.58329261C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046099.1:n.595C>A
Search 100 bp 5'
Search 100 bp 3'