Canonical Allele Identifier: CA511290919

Gene: MIR646HG

Linked Data

• gnomAD v4: 20-60320640-G-T
• MyVariant Identifiers: chr20:g.58895698G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.60320640G>T , CM000682.2:g.60320640G>T	GRCh38
NC_000020.10:g.58895698G>T , CM000682.1:g.58895698G>T	GRCh37
NC_000020.9:g.58329093G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_046099.1:n.427G>T