Canonical Allele Identifier: CA127195579

Gene: MIR3936HG

Linked Data

• dbSNP Id: rs945023111
• gnomAD v3: 5-132369517-G-T
• gnomAD v4: 5-132369517-G-T
• MyVariant Identifiers: chr5:g.131705209G>T (hg19) ; chr5:g.132369517G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132369517G>T , CM000667.2:g.132369517G>T	GRCh38
NC_000005.9:g.131705209G>T , CM000667.1:g.131705209G>T	GRCh37
NC_000005.8:g.131733108G>T	NCBI36
NG_008982.1:g.4809G>T
NG_008982.2:g.4814G>T

Transcript Alleles

HGVS	Amino-acid Change
NR_110997.1:n.73+327C>A