Canonical Allele Identifier: CA127211613

Gene: MIR3936HG

Linked Data

• dbSNP Id: rs930134320
• gnomAD v3: 5-132350578-T-C
• gnomAD v4: 5-132350578-T-C
• MyVariant Identifiers: chr5:g.131686271T>C (hg19) ; chr5:g.132350578T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132350578T>C , CM000667.2:g.132350578T>C	GRCh38
NC_000005.9:g.131686271T>C , CM000667.1:g.131686271T>C	GRCh37
NC_000005.8:g.131714170T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_110997.1:n.418-621A>G