Canonical Allele Identifier: CA989994777
Gene: MIR4527HG HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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