ClinGen Allele Registry
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Canonical Allele Identifier:
CA528537700
Gene: MIR181A1HG
HGNC
NCBI
Linked Data
dbSNP Id:
rs1268833444
gnomAD v2:
1-198867415-T-C
gnomAD v3:
1-198898286-T-C
gnomAD v4:
1-198898286-T-C
MyVariant Identifiers:
chr1:g.198867415T>C (hg19)
chr1:g.198898286T>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.198898286T>C , CM000663.2:g.198898286T>C
GRCh38
NC_000001.10:g.198867415T>C , CM000663.1:g.198867415T>C
GRCh37
NC_000001.9:g.197134038T>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_040073.1:n.363+2125A>G
Search 100 bp 5'
Search 100 bp 3'