Canonical Allele Identifier: CA6084535
Gene: MIR194-2 HGNC NCBI
MIR194-2HG HGNC NCBI
MyVariant.info:
GRCh38 chr11:g.64891364G>A
GRCh37 chr11:g.64658836G>A
gnomAD v2:
11:64658836 G / A
gnomAD v3:
11:64891364 G / A
gnomAD v4:
chr11-64891364-G-A
Joint Max Group AF 0.06281354 (AFR)
Genomes Max Group AF 0.0622082 (AFR)
Exomes Max Group AF 0.06212996 (AFR)
dbSNP:
11231898
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64891364G>A , CM000673.2:g.64891364G>A GRCh38
NC_000011.9:g.64658836G>A , CM000673.1:g.64658836G>A GRCh37
NC_000011.8:g.64415412G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_029829.1:n.76C>T (MIR194-2)
NR_133638.1:n.1843C>T (MIR194-2HG)
NR_133639.1:n.437+1065C>T (MIR194-2HG)
NR_133640.1:n.276+1226C>T (MIR194-2HG)
XR_950199.1:n.778+1065C>T (MIR194-2HG)
XR_950200.1:n.617+1226C>T (MIR194-2HG)
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