Canonical Allele Identifier: CA445378332
Gene: MIR9-2HG HGNC NCBI

Linked Data

dbSNP Id: rs1250760168
gnomAD v2: 5-87968852-A-G
gnomAD v3: 5-88673034-A-G
gnomAD v4: 5-88673034-A-G
MyVariant Identifiers: chr5:g.87968852A>G (hg19) chr5:g.88673034A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.88673034A>G , CM000667.2:g.88673034A>G GRCh38
NC_000005.9:g.87968852A>G , CM000667.1:g.87968852A>G GRCh37
NC_000005.8:g.88004608A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_015436.1:n.147-6T>C
NR_024383.1:n.99-6T>C
NR_024384.1:n.295T>C
NR_015436.2:n.169-6T>C
NR_024383.2:n.102-6T>C
NR_024384.2:n.306T>C
NR_152232.1:n.186T>C
NR_152233.1:n.130-6T>C
NR_152234.1:n.169-6T>C
NR_152235.1:n.169-1949T>C
NR_152236.1:n.225T>C
NR_152237.1:n.169-1949T>C
NR_152238.1:n.102-6T>C
NR_152239.1:n.102-1949T>C
NR_152240.1:n.909T>C
NR_152241.1:n.115T>C
NR_152242.1:n.306T>C
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