Canonical Allele Identifier: CA511291628
Gene: MIR646HG HGNC NCBI

Linked Data

gnomAD v4: 20-60320884-G-A
MyVariant Identifiers: chr20:g.58895942G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.60320884G>A , CM000682.2:g.60320884G>A GRCh38
NC_000020.10:g.58895942G>A , CM000682.1:g.58895942G>A GRCh37
NC_000020.9:g.58329337G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046099.1:n.671G>A
Search 100 bp 5'
Search 100 bp 3'