Canonical Allele Identifier: CA511291540

Gene: MIR646HG

Linked Data

• dbSNP Id: rs1452908052
• gnomAD v3: 20-60320854-C-T
• gnomAD v4: 20-60320854-C-T
• MyVariant Identifiers: chr20:g.58895912C>T (hg19) ; chr20:g.60320854C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.60320854C>T , CM000682.2:g.60320854C>T	GRCh38
NC_000020.10:g.58895912C>T , CM000682.1:g.58895912C>T	GRCh37
NC_000020.9:g.58329307C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_046099.1:n.641C>T