Canonical Allele Identifier: CA14573406

Gene: MIR4527HG

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.47333893G>A , CM000680.2:g.47333893G>A	GRCh38
NC_000018.9:g.44860264G>A , CM000680.1:g.44860264G>A	GRCh37
NC_000018.8:g.43114262G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_147192.1:n.38+48132G>A