Canonical Allele Identifier: CA15149157
Gene: MIR3681HG HGNC NCBI

Linked Data

dbSNP Id: rs10929808
gnomAD v2: 2-12568996-G-A
gnomAD v3: 2-12428870-G-A
gnomAD v4: 2-12428870-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.12428870G>A , CM000664.2:g.12428870G>A GRCh38
NC_000002.11:g.12568996G>A , CM000664.1:g.12568996G>A GRCh37
NC_000002.10:g.12486447G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110196.1:n.424+120086G>A