Canonical Allele Identifier: CA1583129189
Gene: MIR3936HG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132350547T= , CM000667.2:g.132350547T= GRCh38
NC_000005.9:g.131686240T= , CM000667.1:g.131686240T= GRCh37
NC_000005.8:g.131714139T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.418-590A=