Canonical Allele Identifier: CA804017375

Gene: MIR3936HG

Linked Data

• dbSNP Id: rs1285335726
• gnomAD v3: 5-132350515-TAACTC-T
• gnomAD v4: 5-132350515-TAACTC-T
• MyVariant Identifiers: chr5:g.131686209_131686213del (hg19) ; chr5:g.132350516_132350520del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132350518_132350522del , CM000667.2:g.132350518_132350522del	GRCh38
NC_000005.9:g.131686211_131686215del , CM000667.1:g.131686211_131686215del	GRCh37
NC_000005.8:g.131714110_131714114del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_110997.1:n.418-563_418-559del