Canonical Allele Identifier: CA127211605

Gene: MIR3936HG

Linked Data

• dbSNP Id: rs910594232
• gnomAD v3: 5-132350546-A-G
• gnomAD v4: 5-132350546-A-G
• MyVariant Identifiers: chr5:g.131686239A>G (hg19) ; chr5:g.132350546A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132350546A>G , CM000667.2:g.132350546A>G	GRCh38
NC_000005.9:g.131686239A>G , CM000667.1:g.131686239A>G	GRCh37
NC_000005.8:g.131714138A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_110997.1:n.418-589T>C