Canonical Allele Identifier: CA12036584

Gene: MIR3936HG

Linked Data

• ClinVar Variation Id: 1221263
• ClinVar RCV Id: RCV001597452
• dbSNP Id: rs2631369
• gnomAD v2: 5-131705266-G-C
• gnomAD v3: 5-132369574-G-C
• gnomAD v4: 5-132369574-G-C
• MyVariant Identifiers: chr5:g.131705266G>C (hg19) ; chr5:g.132369574G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132369574G>C , CM000667.2:g.132369574G>C	GRCh38
NC_000005.9:g.131705266G>C , CM000667.1:g.131705266G>C	GRCh37
NC_000005.8:g.131733165G>C	NCBI36
NG_008982.1:g.4866G>C
NG_008982.2:g.4871G>C

Transcript Alleles

HGVS	Amino-acid Change
NR_110997.1:n.73+270C>G