Canonical Allele Identifier: CA445378135
Gene: MIR9-2HG HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.87968784T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.88672966T>C , CM000667.2:g.88672966T>C GRCh38
NC_000005.9:g.87968784T>C , CM000667.1:g.87968784T>C GRCh37
NC_000005.8:g.88004540T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_015436.1:n.209A>G
NR_024383.1:n.161A>G
NR_024384.1:n.363A>G
NR_015436.2:n.231A>G
NR_024383.2:n.164A>G
NR_024384.2:n.374A>G
NR_152232.1:n.254A>G
NR_152233.1:n.192A>G
NR_152234.1:n.231A>G
NR_152235.1:n.169-1881A>G
NR_152236.1:n.293A>G
NR_152237.1:n.169-1881A>G
NR_152238.1:n.164A>G
NR_152239.1:n.102-1881A>G
NR_152240.1:n.977A>G
NR_152241.1:n.183A>G
NR_152242.1:n.374A>G
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