Canonical Allele Identifier: CA12004828
Gene: MIR9-2HG HGNC NCBI
COSMIC:
COSN20362449 (not active)
MyVariant.info:
GRCh38 chr5:g.88673046A>G
GRCh37 chr5:g.87968864A>G
gnomAD v2:
5:87968864 A / G
gnomAD v3:
5:88673046 A / G
gnomAD v4:
chr5-88673046-A-G
Joint Max Group AF 0.50177797 (EAS)
Genomes Max Group AF 0.50297949 (EAS)
Exomes Max Group AF 0.41023641 (MID)
dbSNP:
6882046
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.88673046A>G , CM000667.2:g.88673046A>G GRCh38
NC_000005.9:g.87968864A>G , CM000667.1:g.87968864A>G GRCh37
NC_000005.8:g.88004620A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_015436.1:n.147-18T>C
NR_024383.1:n.99-18T>C
NR_024384.1:n.283T>C
NR_015436.2:n.169-18T>C
NR_024383.2:n.102-18T>C
NR_024384.2:n.294T>C
NR_152232.1:n.174T>C
NR_152233.1:n.130-18T>C
NR_152234.1:n.169-18T>C
NR_152235.1:n.169-1961T>C
NR_152236.1:n.213T>C
NR_152237.1:n.169-1961T>C
NR_152238.1:n.102-18T>C
NR_152239.1:n.102-1961T>C
NR_152240.1:n.897T>C
NR_152241.1:n.103T>C
NR_152242.1:n.294T>C
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