Canonical Allele Identifier: CA1081635064

Gene: MIR3936HG

Linked Data

• dbSNP Id: rs998754700
• gnomAD v3: 5-132369683-C-A
• gnomAD v4: 5-132369683-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132369683C>A , CM000667.2:g.132369683C>A	GRCh38
NC_000005.9:g.131705375C>A , CM000667.1:g.131705375C>A	GRCh37
NC_000005.8:g.131733274C>A	NCBI36
NG_008982.1:g.4975C>A
NG_008982.2:g.4980C>A

Transcript Alleles

HGVS	Amino-acid Change
NR_110997.1:n.73+161G>T