Canonical Allele Identifier: CA13450932

Gene: MIR100HG

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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