Canonical Allele Identifier: CA1183130589
Gene: MIR137HG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.98037378G>A , CM000663.2:g.98037378G>A GRCh38
NC_000001.10:g.98502934G>A , CM000663.1:g.98502934G>A GRCh37
NC_000001.9:g.98275522G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046105.1:n.814+8630C>T