Canonical Allele Identifier: CA2489305656
Gene: MIR3681HG HGNC NCBI

Linked Data

dbSNP Id: rs1662015822

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.12112320_12112322del , CM000664.2:g.12112320_12112322del GRCh38
NC_000002.11:g.12252446_12252448del , CM000664.1:g.12252446_12252448del GRCh37
NC_000002.10:g.12169897_12169899del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110196.1:n.210-54418_210-54416del
NR_110197.1:n.343+5369_343+5371del