Canonical Allele Identifier: CA562765051

Gene: MIR3936HG

Linked Data

• dbSNP Id: rs988192066
• gnomAD v2: 5-131686073-G-A
• gnomAD v3: 5-132350380-G-A
• gnomAD v4: 5-132350380-G-A
• MyVariant Identifiers: chr5:g.131686073G>A (hg19) ; chr5:g.132350380G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132350380G>A , CM000667.2:g.132350380G>A	GRCh38
NC_000005.9:g.131686073G>A , CM000667.1:g.131686073G>A	GRCh37
NC_000005.8:g.131713972G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_110997.1:n.418-423C>T