Canonical Allele Identifier: CA2675194457
Gene: MIR3936HG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132369513T>A , CM000667.2:g.132369513T>A GRCh38
NC_000005.9:g.131705205T>A , CM000667.1:g.131705205T>A GRCh37
NC_000005.8:g.131733104T>A NCBI36
NG_008982.1:g.4805T>A
NG_008982.2:g.4810T>A

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.73+331A>T