Canonical Allele Identifier: CA1081635004

Gene: MIR3936HG

Linked Data

• dbSNP Id: rs1751792923
• gnomAD v3: 5-132369587-C-T
• gnomAD v4: 5-132369587-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132369587C>T , CM000667.2:g.132369587C>T	GRCh38
NC_000005.9:g.131705279C>T , CM000667.1:g.131705279C>T	GRCh37
NC_000005.8:g.131733178C>T	NCBI36
NG_008982.1:g.4879C>T
NG_008982.2:g.4884C>T

Transcript Alleles

HGVS	Amino-acid Change
NR_110997.1:n.73+257G>A