Canonical Allele Identifier: CA1583129061
Gene: MIR3936HG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132350187A= , CM000667.2:g.132350187A= GRCh38
NC_000005.9:g.131685880A= , CM000667.1:g.131685880A= GRCh37
NC_000005.8:g.131713779A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.418-230T=