Canonical Allele Identifier: CA804017361

Gene: MIR3936HG

Linked Data

• dbSNP Id: rs1156322009
• MyVariant Identifiers: chr5:g.131686112_131686113del (hg19) ; chr5:g.132350419_132350420del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132350419_132350420del , CM000667.2:g.132350419_132350420del	GRCh38
NC_000005.9:g.131686112_131686113del , CM000667.1:g.131686112_131686113del	GRCh37
NC_000005.8:g.131714011_131714012del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_110997.1:n.418-463_418-462del