Canonical Allele Identifier: CA511291531

Gene: MIR646HG

Linked Data

• dbSNP Id: rs2123093700
• MyVariant Identifiers: chr20:g.58895909C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.60320851C>T , CM000682.2:g.60320851C>T	GRCh38
NC_000020.10:g.58895909C>T , CM000682.1:g.58895909C>T	GRCh37
NC_000020.9:g.58329304C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_046099.1:n.638C>T