Canonical Allele Identifier: CA511290931

Gene: MIR646HG

Linked Data

• gnomAD v4: 20-60320644-C-A
• MyVariant Identifiers: chr20:g.58895702C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.60320644C>A , CM000682.2:g.60320644C>A	GRCh38
NC_000020.10:g.58895702C>A , CM000682.1:g.58895702C>A	GRCh37
NC_000020.9:g.58329097C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_046099.1:n.431C>A