Canonical Allele Identifier: CA1583129131
Gene: MIR3936HG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132350353C= , CM000667.2:g.132350353C= GRCh38
NC_000005.9:g.131686046C= , CM000667.1:g.131686046C= GRCh37
NC_000005.8:g.131713945C= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110997.1:n.418-396G=