Canonical Allele Identifier: CA1583129141

Gene: MIR3936HG

Linked Data

• dbSNP Id: rs1580857179
• gnomAD v3: 5-132350394-T-C
• gnomAD v4: 5-132350394-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132350394T>C , CM000667.2:g.132350394T>C	GRCh38
NC_000005.9:g.131686087T>C , CM000667.1:g.131686087T>C	GRCh37
NC_000005.8:g.131713986T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_110997.1:n.418-437A>G