Canonical Allele Identifier: CA1081635037

Gene: MIR3936HG

Linked Data

• dbSNP Id: rs1751796120
• gnomAD v3: 5-132369636-C-G
• gnomAD v4: 5-132369636-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132369636C>G , CM000667.2:g.132369636C>G	GRCh38
NC_000005.9:g.131705328C>G , CM000667.1:g.131705328C>G	GRCh37
NC_000005.8:g.131733227C>G	NCBI36
NG_008982.1:g.4928C>G
NG_008982.2:g.4933C>G

Transcript Alleles

HGVS	Amino-acid Change
NR_110997.1:n.73+208G>C