Canonical Allele Identifier: CA2489305619
Gene: MIR3681HG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.12112237T= , CM000664.2:g.12112237T= GRCh38
NC_000002.11:g.12252363T= , CM000664.1:g.12252363T= GRCh37
NC_000002.10:g.12169814T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110196.1:n.210-54501T=
NR_110197.1:n.343+5286T=