Canonical Allele Identifier: CA317000067

Gene: MIR646HG

Linked Data

• dbSNP Id: rs943257036
• gnomAD v2: 20-58895885-G-A
• gnomAD v3: 20-60320827-G-A
• gnomAD v4: 20-60320827-G-A
• MyVariant Identifiers: chr20:g.58895885G>A (hg19) ; chr20:g.60320827G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.60320827G>A , CM000682.2:g.60320827G>A	GRCh38
NC_000020.10:g.58895885G>A , CM000682.1:g.58895885G>A	GRCh37
NC_000020.9:g.58329280G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_046099.1:n.614G>A