Canonical Allele Identifier: CA562765055

Gene: MIR3936HG

Linked Data

• dbSNP Id: rs1198636209
• gnomAD v2: 5-131686209-A-T
• gnomAD v3: 5-132350516-A-T
• gnomAD v4: 5-132350516-A-T
• MyVariant Identifiers: chr5:g.131686209A>T (hg19) ; chr5:g.132350516A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132350516A>T , CM000667.2:g.132350516A>T	GRCh38
NC_000005.9:g.131686209A>T , CM000667.1:g.131686209A>T	GRCh37
NC_000005.8:g.131714108A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_110997.1:n.418-559T>A