Canonical Allele Identifier: CA511291585

Gene: MIR646HG

Linked Data

• dbSNP Id: rs1731300190
• MyVariant Identifiers: chr20:g.58895928C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.60320870C>G , CM000682.2:g.60320870C>G	GRCh38
NC_000020.10:g.58895928C>G , CM000682.1:g.58895928C>G	GRCh37
NC_000020.9:g.58329323C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_046099.1:n.657C>G