Canonical Allele Identifier: CA1583129135
Gene: MIR3936HG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132350368G= , CM000667.2:g.132350368G= GRCh38
NC_000005.9:g.131686061G= , CM000667.1:g.131686061G= GRCh37
NC_000005.8:g.131713960G= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110997.1:n.418-411C=