Canonical Allele Identifier: CA317000077
Gene: MIR646HG HGNC NCBI

Linked Data

dbSNP Id: rs936396857
gnomAD v2: 20-58895975-A-T
gnomAD v3: 20-60320917-A-T
gnomAD v4: 20-60320917-A-T
MyVariant Identifiers: chr20:g.58895975A>T (hg19) chr20:g.60320917A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.60320917A>T , CM000682.2:g.60320917A>T GRCh38
NC_000020.10:g.58895975A>T , CM000682.1:g.58895975A>T GRCh37
NC_000020.9:g.58329370A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046099.1:n.704A>T
Search 100 bp 5'
Search 100 bp 3'