Canonical Allele Identifier: CA127211562

Gene: MIR3936HG

Linked Data

• dbSNP Id: rs552210474
• gnomAD v3: 5-132350311-C-T
• gnomAD v4: 5-132350311-C-T
• MyVariant Identifiers: chr5:g.131686004C>T (hg19) ; chr5:g.132350311C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132350311C>T , CM000667.2:g.132350311C>T	GRCh38
NC_000005.9:g.131686004C>T , CM000667.1:g.131686004C>T	GRCh37
NC_000005.8:g.131713903C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_110997.1:n.418-354G>A