Canonical Allele Identifier: CA803979927

Gene: MIR3936HG

Linked Data

• dbSNP Id: rs1054900555
• gnomAD v4: 5-132369627-C-A
• MyVariant Identifiers: chr5:g.131705319C>A (hg19) ; chr5:g.132369627C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132369627C>A , CM000667.2:g.132369627C>A	GRCh38
NC_000005.9:g.131705319C>A , CM000667.1:g.131705319C>A	GRCh37
NC_000005.8:g.131733218C>A	NCBI36
NG_008982.1:g.4919C>A
NG_008982.2:g.4924C>A

Transcript Alleles

HGVS	Amino-acid Change
NR_110997.1:n.73+217G>T