Canonical Allele Identifier: CA729929063

Gene: MIR181A1HG

Linked Data

• dbSNP Id: rs1200412039
• gnomAD v3: 1-198898476-CCTT-C
• gnomAD v4: 1-198898476-CCTT-C
• MyVariant Identifiers: chr1:g.198867606_198867608del (hg19) ; chr1:g.198898477_198898479del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.198898480_198898482del , CM000663.2:g.198898480_198898482del	GRCh38
NC_000001.10:g.198867609_198867611del , CM000663.1:g.198867609_198867611del	GRCh37
NC_000001.9:g.197134232_197134234del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040073.1:n.363+1932_363+1934del