Canonical Allele Identifier: CA2489305632
Gene: MIR3681HG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.12112267C= , CM000664.2:g.12112267C= GRCh38
NC_000002.11:g.12252393C= , CM000664.1:g.12252393C= GRCh37
NC_000002.10:g.12169844C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110196.1:n.210-54471C=
NR_110197.1:n.343+5316C=