Allele Registry

Canonical Allele Identifier: CA15149157

Gene: MIR3681HG HGNC NCBI

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr2:g.12428870G>A

GRCh37 chr2:g.12568996G>A

Linked Data - Sequence & Population

gnomAD v2:

2:12568996 G / A

gnomAD v3:

2:12428870 G / A

gnomAD v4:

chr2-12428870-G-A

Joint Max Group AF 0.89122576 (AFR)

Genomes Max Group AF 0.89122576 (AFR)

Linked Data - NCBI & NCI

dbSNP:

10929808

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

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