Canonical Allele Identifier: CA562767590

Gene: MIR3936HG

Linked Data

• dbSNP Id: rs1176581185
• gnomAD v2: 5-131705323-A-C
• gnomAD v3: 5-132369631-A-C
• gnomAD v4: 5-132369631-A-C
• MyVariant Identifiers: chr5:g.131705323A>C (hg19) ; chr5:g.132369631A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132369631A>C , CM000667.2:g.132369631A>C	GRCh38
NC_000005.9:g.131705323A>C , CM000667.1:g.131705323A>C	GRCh37
NC_000005.8:g.131733222A>C	NCBI36
NG_008982.1:g.4923A>C
NG_008982.2:g.4928A>C

Transcript Alleles

HGVS	Amino-acid Change
NR_110997.1:n.73+213T>G