Canonical Allele Identifier: CA27778642
Gene: MIR137HG HGNC NCBI
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Genomic Alleles

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

Transcript Alleles

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