Canonical Allele Identifier: CA15074967
Gene: MIR181A1HG HGNC NCBI

Linked Data

ClinVar Variation Id: 427754
ClinVar RCV Id: RCV001777167
dbSNP Id: rs60639710
gnomAD v2: 1-198867678-G-T
gnomAD v3: 1-198898549-G-T
gnomAD v4: 1-198898549-G-T
MyVariant Identifiers: chr1:g.198867678G>T (hg19) chr1:g.198898549G>T (hg38)
PubMed: PMID:29254171
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.198898549G>T , CM000663.2:g.198898549G>T GRCh38
NC_000001.10:g.198867678G>T , CM000663.1:g.198867678G>T GRCh37
NC_000001.9:g.197134301G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_040073.1:n.363+1862C>A
Search 100 bp 5'
Search 100 bp 3'