Canonical Allele Identifier: CA1583135783
Gene: MIR3936HG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132358913G>T , CM000667.2:g.132358913G>T GRCh38
NC_000005.9:g.131694606G>T , CM000667.1:g.131694606G>T GRCh37
NC_000005.8:g.131722505G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.417+1167C>A