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Canonical Allele Identifier:
CA11000793
Gene: MIR3681HG
HGNC
NCBI
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr2:g.12500615G>A
GRCh37
chr2:g.12640741G>A
Linked Data - Sequence & Population
gnomAD v2:
2:12640741 G / A
gnomAD v3:
2:12500615 G / A
gnomAD v4:
chr2-12500615-G-A
Joint Max Group AF
0.70619116 (EAS)
Genomes Max Group AF
0.70619116 (EAS)
Linked Data - NCBI & NCI
dbSNP:
1534422
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.12500615G>A , CM000664.2:g.12500615G>A
GRCh38
NC_000002.11:g.12640741G>A , CM000664.1:g.12640741G>A
GRCh37
NC_000002.10:g.12558192G>A
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_110196.1:n.425-57591G>A
Search 100 bp 5'
Search 100 bp 3'