Canonical Allele Identifier: CA1583129165
Gene: MIR3936HG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132350452T= , CM000667.2:g.132350452T= GRCh38
NC_000005.9:g.131686145T= , CM000667.1:g.131686145T= GRCh37
NC_000005.8:g.131714044T= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110997.1:n.418-495A=