Canonical Allele Identifier: CA562765053

Gene: MIR3936HG

Linked Data

• dbSNP Id: rs1342808962
• gnomAD v2: 5-131686123-AATTTT-A
• MyVariant Identifiers: chr5:g.131686124_131686128del (hg19) ; chr5:g.132350431_132350435del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132350432_132350436del , CM000667.2:g.132350432_132350436del	GRCh38
NC_000005.9:g.131686125_131686129del , CM000667.1:g.131686125_131686129del	GRCh37
NC_000005.8:g.131714024_131714028del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_110997.1:n.418-478_418-474del