Canonical Allele Identifier: CA10854753
Gene: MIR181A1HG HGNC NCBI

Linked Data

ClinVar Variation Id: 427756
dbSNP Id: rs10800598

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