Canonical Allele Identifier: CA511291677
Gene: MIR646HG HGNC NCBI

Linked Data

gnomAD v4: 20-60320901-T-A
MyVariant Identifiers: chr20:g.58895959T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.60320901T>A , CM000682.2:g.60320901T>A GRCh38
NC_000020.10:g.58895959T>A , CM000682.1:g.58895959T>A GRCh37
NC_000020.9:g.58329354T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046099.1:n.688T>A
Search 100 bp 5'
Search 100 bp 3'