Canonical Allele Identifier: CA2710090329
Gene: MIR3936HG HGNC NCBI

Linked Data

dbSNP Id: rs1580857229

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132350566C>G , CM000667.2:g.132350566C>G GRCh38
NC_000005.9:g.131686259C>G , CM000667.1:g.131686259C>G GRCh37
NC_000005.8:g.131714158C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.418-609G>C