Canonical Allele Identifier: CA562765052

Gene: MIR3936HG

Linked Data

• dbSNP Id: rs1255151136
• gnomAD v2: 5-131686119-A-G
• gnomAD v3: 5-132350426-A-G
• gnomAD v4: 5-132350426-A-G
• MyVariant Identifiers: chr5:g.131686119A>G (hg19) ; chr5:g.132350426A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132350426A>G , CM000667.2:g.132350426A>G	GRCh38
NC_000005.9:g.131686119A>G , CM000667.1:g.131686119A>G	GRCh37
NC_000005.8:g.131714018A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_110997.1:n.418-469T>C