Canonical Allele Identifier: CA1081639551

Gene: MIR3936HG

Linked Data

• dbSNP Id: rs1373858364
• gnomAD v3: 5-132350368-G-T
• gnomAD v4: 5-132350368-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132350368G>T , CM000667.2:g.132350368G>T	GRCh38
NC_000005.9:g.131686061G>T , CM000667.1:g.131686061G>T	GRCh37
NC_000005.8:g.131713960G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_110997.1:n.418-411C>A