Canonical Allele Identifier: CA13544274

Gene: MIR100HG

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.122083949G>A , CM000673.2:g.122083949G>A	GRCh38
NC_000011.9:g.121954657G>A , CM000673.1:g.121954657G>A	GRCh37
NC_000011.8:g.121459867G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_137178.1:n.473+16425C>T