Canonical Allele Identifier: CA942992989
Gene: MIR100HG HGNC NCBI
gnomAD v3:
11:122168344 T / C
gnomAD v4:
chr11-122168344-T-C
Joint Max Group AF 0.00007299 (SAS)
Genomes Max Group AF 0.00007299 (SAS)
dbSNP:
11218544
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.122168344T>C , CM000673.2:g.122168344T>C GRCh38
NC_000011.9:g.122039052T>C , CM000673.1:g.122039052T>C GRCh37
NC_000011.8:g.121544262T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_024430.1:n.362+11992A>G
NR_024430.2:n.409+11992A>G
NR_137179.1:n.363+11992A>G
NR_137180.1:n.421+11992A>G
NR_137181.1:n.409+11992A>G
NR_137182.1:n.409+11992A>G
NR_137183.1:n.297+11992A>G
NR_137184.1:n.297+11992A>G
NR_137185.1:n.297+11992A>G
NR_137192.1:n.676+11992A>G
NR_137193.1:n.421+11992A>G
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