Canonical Allele Identifier: CA317000052
Gene: MIR646HG HGNC NCBI

Linked Data

dbSNP Id: rs574973278
gnomAD v2: 20-58895783-T-A
gnomAD v3: 20-60320725-T-A
gnomAD v4: 20-60320725-T-A
MyVariant Identifiers: chr20:g.58895783T>A (hg19) chr20:g.60320725T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.60320725T>A , CM000682.2:g.60320725T>A GRCh38
NC_000020.10:g.58895783T>A , CM000682.1:g.58895783T>A GRCh37
NC_000020.9:g.58329178T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046099.1:n.512T>A
Search 100 bp 5'
Search 100 bp 3'