Canonical Allele Identifier: CA1583129188
Gene: MIR3936HG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132350546A= , CM000667.2:g.132350546A= GRCh38
NC_000005.9:g.131686239A= , CM000667.1:g.131686239A= GRCh37
NC_000005.8:g.131714138A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.418-589T=