Canonical Allele Identifier: CA16549377

Gene: MIR3976HG

Linked Data

• dbSNP Id: rs11662763
• gnomAD v2: 18-5857091-C-T
• gnomAD v3: 18-5857092-C-T
• gnomAD v4: 18-5857092-C-T
• MyVariant Identifiers: chr18:g.5857091C>T (hg19) ; chr18:g.5857092C>T (hg38)
• Allelic Epigenome: Alellic Epigenome (raw data)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.5857092C>T , CM000680.2:g.5857092C>T	GRCh38
NC_000018.9:g.5857091C>T , CM000680.1:g.5857091C>T	GRCh37
NC_000018.8:g.5847091C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_172494.1:n.603-21351C>T
NR_172495.1:n.603-19161C>T
NR_172496.1:n.603-19161C>T
NR_172497.1:n.603-19161C>T
NR_172498.1:n.663-10021C>T
NR_172499.1:n.603-19161C>T
NR_172500.1:n.603-19161C>T
NR_172501.1:n.603-19161C>T
NR_172502.1:n.603-19161C>T
NR_172503.1:n.603-19161C>T