Canonical Allele Identifier: CA127211572

Gene: MIR3936HG

Linked Data

• dbSNP Id: rs552072256
• gnomAD v2: 5-131686053-T-TA
• gnomAD v3: 5-132350360-T-TA
• gnomAD v4: 5-132350360-T-TA
• MyVariant Identifiers: chr5:g.131686053_131686054insA (hg19) ; chr5:g.132350360_132350361insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132350362dup , CM000667.2:g.132350362dup	GRCh38
NC_000005.9:g.131686055dup , CM000667.1:g.131686055dup	GRCh37
NC_000005.8:g.131713954dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_110997.1:n.418-404dup