Canonical Allele Identifier: CA740834890
Gene: MIR137HG HGNC NCBI

Linked Data

dbSNP Id: rs1702294

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.98036428T>A , CM000663.2:g.98036428T>A GRCh38
NC_000001.10:g.98501984T>A , CM000663.1:g.98501984T>A GRCh37
NC_000001.9:g.98274572T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_046105.1:n.814+9580A>T