Canonical Allele Identifier: CA1183116345
Gene: MIR137HG HGNC NCBI

Linked Data

dbSNP Id: rs1675788794

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.98006111A>G , CM000663.2:g.98006111A>G GRCh38
NC_000001.10:g.98471667A>G , CM000663.1:g.98471667A>G GRCh37
NC_000001.9:g.98244255A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046105.1:n.815-11111T>C