Canonical Allele Identifier: CA1583129136
Gene: MIR3936HG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132350372A= , CM000667.2:g.132350372A= GRCh38
NC_000005.9:g.131686065A= , CM000667.1:g.131686065A= GRCh37
NC_000005.8:g.131713964A= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110997.1:n.418-415T=