Canonical Allele Identifier: CA15991048

Gene: MIR155HG

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25571713A>G , CM000683.2:g.25571713A>G	GRCh38
NC_000021.8:g.26944025A>G , CM000683.1:g.26944025A>G	GRCh37
NC_000021.7:g.25865896A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_001458.3:n.198+1792A>G