Canonical Allele Identifier: CA1081639583

Gene: MIR3936HG

Linked Data

• dbSNP Id: rs1751416496
• gnomAD v3: 5-132350544-A-C
• gnomAD v4: 5-132350544-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132350544A>C , CM000667.2:g.132350544A>C	GRCh38
NC_000005.9:g.131686237A>C , CM000667.1:g.131686237A>C	GRCh37
NC_000005.8:g.131714136A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_110997.1:n.418-587T>G