Canonical Allele Identifier: CA127211576

Gene: MIR3936HG

Linked Data

• dbSNP Id: rs976024933
• gnomAD v3: 5-132350378-T-G
• gnomAD v4: 5-132350378-T-G
• MyVariant Identifiers: chr5:g.131686071T>G (hg19) ; chr5:g.132350378T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132350378T>G , CM000667.2:g.132350378T>G	GRCh38
NC_000005.9:g.131686071T>G , CM000667.1:g.131686071T>G	GRCh37
NC_000005.8:g.131713970T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_110997.1:n.418-421A>C