Canonical Allele Identifier: CA562765050

Gene: MIR3936HG

Linked Data

• dbSNP Id: rs1311721609
• gnomAD v2: 5-131686069-AAT-A
• gnomAD v3: 5-132350376-AAT-A
• gnomAD v4: 5-132350376-AAT-A
• MyVariant Identifiers: chr5:g.131686070_131686071del (hg19) ; chr5:g.132350377_132350378del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132350378_132350379del , CM000667.2:g.132350378_132350379del	GRCh38
NC_000005.9:g.131686071_131686072del , CM000667.1:g.131686071_131686072del	GRCh37
NC_000005.8:g.131713970_131713971del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_110997.1:n.418-421_418-420del