Canonical Allele Identifier: CA562765056

Gene: MIR3936HG

Linked Data

• dbSNP Id: rs1376233855
• gnomAD v2: 5-131686234-A-T
• gnomAD v3: 5-132350541-A-T
• gnomAD v4: 5-132350541-A-T
• MyVariant Identifiers: chr5:g.131686234A>T (hg19) ; chr5:g.132350541A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132350541A>T , CM000667.2:g.132350541A>T	GRCh38
NC_000005.9:g.131686234A>T , CM000667.1:g.131686234A>T	GRCh37
NC_000005.8:g.131714133A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_110997.1:n.418-584T>A