Canonical Allele Identifier: CA756007534
Gene: MIR3681HG HGNC NCBI

Linked Data

dbSNP Id: rs1418550646
gnomAD v3: 2-12112257-G-T
gnomAD v4: 2-12112257-G-T
MyVariant Identifiers: chr2:g.12252383G>T (hg19) chr2:g.12112257G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.12112257G>T , CM000664.2:g.12112257G>T GRCh38
NC_000002.11:g.12252383G>T , CM000664.1:g.12252383G>T GRCh37
NC_000002.10:g.12169834G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110196.1:n.210-54481G>T
NR_110197.1:n.343+5306G>T
Search 100 bp 5'
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