Canonical Allele Identifier: CA11108639

Gene: MIR3681HG

Linked Data

• dbSNP Id: rs17551536
• gnomAD v2: 2-12252350-A-G
• gnomAD v3: 2-12112224-A-G
• gnomAD v4: 2-12112224-A-G
• MyVariant Identifiers: chr2:g.12252350A>G (hg19) ; chr2:g.12112224A>G (hg38)

Genomic Alleles

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

Transcript Alleles

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