Canonical Allele Identifier: CA511291135
Gene: MIR646HG HGNC NCBI

Linked Data

dbSNP Id: rs1373739980
MyVariant Identifiers: chr20:g.58895771G>A (hg19) chr20:g.60320713G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.60320713G>A , CM000682.2:g.60320713G>A GRCh38
NC_000020.10:g.58895771G>A , CM000682.1:g.58895771G>A GRCh37
NC_000020.9:g.58329166G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046099.1:n.500G>A
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