Canonical Allele Identifier: CA2489455334
Gene: MIR3681HG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.12428870G= , CM000664.2:g.12428870G= GRCh38
NC_000002.11:g.12568996G= , CM000664.1:g.12568996G= GRCh37
NC_000002.10:g.12486447G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110196.1:n.424+120086G=