Canonical Allele Identifier: CA122602422
Gene: MIR9-2HG HGNC NCBI

Linked Data

dbSNP Id: rs1029127348
MyVariant Identifiers: chr5:g.87968762G>C (hg19) chr5:g.88672944G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.88672944G>C , CM000667.2:g.88672944G>C GRCh38
NC_000005.9:g.87968762G>C , CM000667.1:g.87968762G>C GRCh37
NC_000005.8:g.88004518G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_015436.1:n.210+21C>G
NR_024383.1:n.162+21C>G
NR_024384.1:n.364+21C>G
NR_015436.2:n.232+21C>G
NR_024383.2:n.165+21C>G
NR_024384.2:n.375+21C>G
NR_152232.1:n.255+21C>G
NR_152233.1:n.193+21C>G
NR_152234.1:n.232+21C>G
NR_152235.1:n.169-1859C>G
NR_152236.1:n.294+21C>G
NR_152237.1:n.169-1859C>G
NR_152238.1:n.165+21C>G
NR_152239.1:n.102-1859C>G
NR_152240.1:n.978+21C>G
NR_152241.1:n.184+21C>G
NR_152242.1:n.375+21C>G
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