Canonical Allele Identifier: CA1583137353

Gene: MIR3936HG

Linked Data

• dbSNP Id: rs1751795338
• gnomAD v4: 5-132369623-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132369623G>A , CM000667.2:g.132369623G>A	GRCh38
NC_000005.9:g.131705315G>A , CM000667.1:g.131705315G>A	GRCh37
NC_000005.8:g.131733214G>A	NCBI36
NG_008982.1:g.4915G>A
NG_008982.2:g.4920G>A

Transcript Alleles

HGVS	Amino-acid Change
NR_110997.1:n.73+221C>T