Canonical Allele Identifier: CA1081639523
Gene: MIR3936HG HGNC NCBI

Linked Data

dbSNP Id: rs1751413618

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132350290G>T , CM000667.2:g.132350290G>T GRCh38
NC_000005.9:g.131685983G>T , CM000667.1:g.131685983G>T GRCh37
NC_000005.8:g.131713882G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.418-333C>A