Canonical Allele Identifier: CA317000045
Gene: MIR646HG HGNC NCBI

Linked Data

dbSNP Id: rs559004041
gnomAD v3: 20-60320638-C-G
gnomAD v4: 20-60320638-C-G
MyVariant Identifiers: chr20:g.58895696C>G (hg19) chr20:g.60320638C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.60320638C>G , CM000682.2:g.60320638C>G GRCh38
NC_000020.10:g.58895696C>G , CM000682.1:g.58895696C>G GRCh37
NC_000020.9:g.58329091C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046099.1:n.425C>G
Search 100 bp 5'
Search 100 bp 3'