Canonical Allele Identifier: CA511291442
Gene: MIR646HG HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.58895879A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.60320821A>C , CM000682.2:g.60320821A>C GRCh38
NC_000020.10:g.58895879A>C , CM000682.1:g.58895879A>C GRCh37
NC_000020.9:g.58329274A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046099.1:n.608A>C