Canonical Allele Identifier: CA804017382

Gene: MIR3936HG

Linked Data

• dbSNP Id: rs1329709897
• MyVariant Identifiers: chr5:g.131686261del (hg19) ; chr5:g.132350568del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132350570del , CM000667.2:g.132350570del	GRCh38
NC_000005.9:g.131686263del , CM000667.1:g.131686263del	GRCh37
NC_000005.8:g.131714162del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_110997.1:n.418-611del