Canonical Allele Identifier: CA1583129157
Gene: MIR3936HG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132350424A= , CM000667.2:g.132350424A= GRCh38
NC_000005.9:g.131686117A= , CM000667.1:g.131686117A= GRCh37
NC_000005.8:g.131714016A= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110997.1:n.418-467T=