Canonical Allele Identifier: CA1078527000
Gene: MIR9-2HG HGNC NCBI

Linked Data

dbSNP Id: rs6893807
gnomAD v3: 5-88669203-A-C
gnomAD v4: 5-88669203-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.88669203A>C , CM000667.2:g.88669203A>C GRCh38
NC_000005.9:g.87965021A>C , CM000667.1:g.87965021A>C GRCh37
NC_000005.8:g.88000777A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_015436.1:n.260+1833T>G
NR_024383.1:n.213-1612T>G
NR_024384.1:n.415-1612T>G
NR_015436.2:n.282+1833T>G
NR_024383.2:n.216-1612T>G
NR_024384.2:n.426-1612T>G
NR_152232.1:n.306-1612T>G
NR_152233.1:n.244-1612T>G
NR_152234.1:n.283-1612T>G
NR_152235.1:n.218+1833T>G
NR_152236.1:n.345-1612T>G
NR_152237.1:n.219-1612T>G
NR_152238.1:n.215+1833T>G
NR_152239.1:n.151+1833T>G
NR_152240.1:n.1029-1612T>G
NR_152241.1:n.235-1612T>G
NR_152242.1:n.425+1833T>G
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