Canonical Allele Identifier: CA815176015
Gene: MIR9-2HG HGNC NCBI

Linked Data

dbSNP Id: rs1455570408
gnomAD v3: 5-88672951-G-A
gnomAD v4: 5-88672951-G-A
MyVariant Identifiers: chr5:g.87968769G>A (hg19) chr5:g.88672951G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.88672951G>A , CM000667.2:g.88672951G>A GRCh38
NC_000005.9:g.87968769G>A , CM000667.1:g.87968769G>A GRCh37
NC_000005.8:g.88004525G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_015436.1:n.210+14C>T
NR_024383.1:n.162+14C>T
NR_024384.1:n.364+14C>T
NR_015436.2:n.232+14C>T
NR_024383.2:n.165+14C>T
NR_024384.2:n.375+14C>T
NR_152232.1:n.255+14C>T
NR_152233.1:n.193+14C>T
NR_152234.1:n.232+14C>T
NR_152235.1:n.169-1866C>T
NR_152236.1:n.294+14C>T
NR_152237.1:n.169-1866C>T
NR_152238.1:n.165+14C>T
NR_152239.1:n.102-1866C>T
NR_152240.1:n.978+14C>T
NR_152241.1:n.184+14C>T
NR_152242.1:n.375+14C>T
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