Canonical Allele Identifier: CA804017347

Gene: MIR3936HG

Linked Data

• dbSNP Id: rs1308631365
• gnomAD v3: 5-132350355-AAATGT-A
• gnomAD v4: 5-132350355-AAATGT-A
• MyVariant Identifiers: chr5:g.131686049_131686053del (hg19) ; chr5:g.132350356_132350360del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132350359_132350363del , CM000667.2:g.132350359_132350363del	GRCh38
NC_000005.9:g.131686052_131686056del , CM000667.1:g.131686052_131686056del	GRCh37
NC_000005.8:g.131713951_131713955del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_110997.1:n.418-403_418-399del