Canonical Allele Identifier: CA127195698

Gene: MIR3936HG

Linked Data

• dbSNP Id: rs937799028
• gnomAD v2: 5-131705313-G-A
• gnomAD v3: 5-132369621-G-A
• gnomAD v4: 5-132369621-G-A
• MyVariant Identifiers: chr5:g.131705313G>A (hg19) ; chr5:g.132369621G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132369621G>A , CM000667.2:g.132369621G>A	GRCh38
NC_000005.9:g.131705313G>A , CM000667.1:g.131705313G>A	GRCh37
NC_000005.8:g.131733212G>A	NCBI36
NG_008982.1:g.4913G>A
NG_008982.2:g.4918G>A

Transcript Alleles

HGVS	Amino-acid Change
NR_110997.1:n.73+223C>T