Canonical Allele Identifier: CA562767551

Gene: MIR3936HG

Linked Data

• dbSNP Id: rs1467441858
• gnomAD v2: 5-131705235-G-A
• gnomAD v3: 5-132369543-G-A
• gnomAD v4: 5-132369543-G-A
• MyVariant Identifiers: chr5:g.131705235G>A (hg19) ; chr5:g.132369543G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132369543G>A , CM000667.2:g.132369543G>A	GRCh38
NC_000005.9:g.131705235G>A , CM000667.1:g.131705235G>A	GRCh37
NC_000005.8:g.131733134G>A	NCBI36
NG_008982.1:g.4835G>A
NG_008982.2:g.4840G>A

Transcript Alleles

HGVS	Amino-acid Change
NR_110997.1:n.73+301C>T