Canonical Allele Identifier: CA1583129138
Gene: MIR3936HG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132350378T= , CM000667.2:g.132350378T= GRCh38
NC_000005.9:g.131686071T= , CM000667.1:g.131686071T= GRCh37
NC_000005.8:g.131713970T= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110997.1:n.418-421A=