Canonical Allele Identifier: CA2489305616
Gene: MIR3681HG HGNC NCBI

Linked Data

dbSNP Id: rs17551536

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.12112224A>C , CM000664.2:g.12112224A>C GRCh38
NC_000002.11:g.12252350A>C , CM000664.1:g.12252350A>C GRCh37
NC_000002.10:g.12169801A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110196.1:n.210-54514A>C
NR_110197.1:n.343+5273A>C