ClinGen Allele Registry
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Canonical Allele Identifier:
CA10854753
Gene: MIR181A1HG
HGNC
NCBI
Linked Data
ClinVar Variation Id:
427756
ClinVar RCV Id:
RCV000509077
RCV001777169
dbSNP Id:
rs10800598
gnomAD v2:
1-198869514-T-C
gnomAD v3:
1-198900385-T-C
gnomAD v4:
1-198900385-T-C
MyVariant Identifiers:
chr1:g.198869514T>C (hg19)
chr1:g.198900385T>C (hg38)
PubMed:
PMID:29254171
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.198900385T>C , CM000663.2:g.198900385T>C
GRCh38
NC_000001.10:g.198869514T>C , CM000663.1:g.198869514T>C
GRCh37
NC_000001.9:g.197136137T>C
NCBI36
Transcript Alleles
HGVS
Amino-acid change
NR_040073.1:n.363+26A>G
Search 100 bp 5'
Search 100 bp 3'