Canonical Allele Identifier: CA127211583

Gene: MIR3936HG

Linked Data

• dbSNP Id: rs537619689
• gnomAD v2: 5-131686117-A-C
• gnomAD v3: 5-132350424-A-C
• gnomAD v4: 5-132350424-A-C
• MyVariant Identifiers: chr5:g.131686117A>C (hg19) ; chr5:g.132350424A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132350424A>C , CM000667.2:g.132350424A>C	GRCh38
NC_000005.9:g.131686117A>C , CM000667.1:g.131686117A>C	GRCh37
NC_000005.8:g.131714016A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_110997.1:n.418-467T>G