Canonical Allele Identifier: CA445378144
Gene: MIR9-2HG HGNC NCBI

Linked Data

gnomAD v4: 5-88672969-T-C
MyVariant Identifiers: chr5:g.87968787T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.88672969T>C , CM000667.2:g.88672969T>C GRCh38
NC_000005.9:g.87968787T>C , CM000667.1:g.87968787T>C GRCh37
NC_000005.8:g.88004543T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_015436.1:n.206A>G
NR_024383.1:n.158A>G
NR_024384.1:n.360A>G
NR_015436.2:n.228A>G
NR_024383.2:n.161A>G
NR_024384.2:n.371A>G
NR_152232.1:n.251A>G
NR_152233.1:n.189A>G
NR_152234.1:n.228A>G
NR_152235.1:n.169-1884A>G
NR_152236.1:n.290A>G
NR_152237.1:n.169-1884A>G
NR_152238.1:n.161A>G
NR_152239.1:n.102-1884A>G
NR_152240.1:n.974A>G
NR_152241.1:n.180A>G
NR_152242.1:n.371A>G