ClinGen Allele Registry
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Canonical Allele Identifier:
CA422742907
Gene: MIR181A1HG
HGNC
NCBI
Linked Data
dbSNP Id:
rs1658080587
gnomAD v3:
1-198898468-T-A
gnomAD v4:
1-198898468-T-A
MyVariant Identifiers:
chr1:g.198867597T>A (hg19)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.198898468T>A , CM000663.2:g.198898468T>A
GRCh38
NC_000001.10:g.198867597T>A , CM000663.1:g.198867597T>A
GRCh37
NC_000001.9:g.197134220T>A
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_040073.1:n.363+1943A>T
Search 100 bp 5'
Search 100 bp 3'