Canonical Allele Identifier: CA804017348

Gene: MIR3936HG

Linked Data

• dbSNP Id: rs1373858364
• gnomAD v3: 5-132350368-G-A
• gnomAD v4: 5-132350368-G-A
• MyVariant Identifiers: chr5:g.131686061G>A (hg19) ; chr5:g.132350368G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132350368G>A , CM000667.2:g.132350368G>A	GRCh38
NC_000005.9:g.131686061G>A , CM000667.1:g.131686061G>A	GRCh37
NC_000005.8:g.131713960G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_110997.1:n.418-411C>T