Canonical Allele Identifier: CA1081635042

Gene: MIR3936HG

Linked Data

• dbSNP Id: rs1751796200
• gnomAD v3: 5-132369637-C-G
• gnomAD v4: 5-132369637-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132369637C>G , CM000667.2:g.132369637C>G	GRCh38
NC_000005.9:g.131705329C>G , CM000667.1:g.131705329C>G	GRCh37
NC_000005.8:g.131733228C>G	NCBI36
NG_008982.1:g.4929C>G
NG_008982.2:g.4934C>G

Transcript Alleles

HGVS	Amino-acid Change
NR_110997.1:n.73+207G>C