Canonical Allele Identifier: CA127195720

Gene: MIR3936HG

Linked Data

• ClinVar Variation Id: 1140554
• ClinVar RCV Id: RCV001477660
• dbSNP Id: rs60978556
• gnomAD v2: 5-131705346-C-A
• gnomAD v3: 5-132369654-C-A
• gnomAD v4: 5-132369654-C-A
• MyVariant Identifiers: chr5:g.131705346C>A (hg19) ; chr5:g.132369654C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132369654C>A , CM000667.2:g.132369654C>A	GRCh38
NC_000005.9:g.131705346C>A , CM000667.1:g.131705346C>A	GRCh37
NC_000005.8:g.131733245C>A	NCBI36
NG_008982.1:g.4946C>A
NG_008982.2:g.4951C>A

Transcript Alleles

HGVS	Amino-acid Change
NR_110997.1:n.73+190G>T