Canonical Allele Identifier: CA2489489955
Gene: MIR3681HG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.12500615G= , CM000664.2:g.12500615G= GRCh38
NC_000002.11:g.12640741G= , CM000664.1:g.12640741G= GRCh37
NC_000002.10:g.12558192G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110196.1:n.425-57591G=