Canonical Allele Identifier: CA127211603

Gene: MIR3936HG

Linked Data

• dbSNP Id: rs190098214
• gnomAD v2: 5-131686192-C-A
• gnomAD v3: 5-132350499-C-A
• gnomAD v4: 5-132350499-C-A
• MyVariant Identifiers: chr5:g.131686192C>A (hg19) ; chr5:g.132350499C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132350499C>A , CM000667.2:g.132350499C>A	GRCh38
NC_000005.9:g.131686192C>A , CM000667.1:g.131686192C>A	GRCh37
NC_000005.8:g.131714091C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_110997.1:n.418-542G>T