Canonical Allele Identifier: CA917584191
Gene: MIR3936HG HGNC NCBI

Linked Data

dbSNP Id: rs1580857146

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132350329del , CM000667.2:g.132350329del GRCh38
NC_000005.9:g.131686022del , CM000667.1:g.131686022del GRCh37
NC_000005.8:g.131713921del NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110997.1:n.418-370del