Canonical Allele Identifier: CA422743747
Gene: MIR181A1HG HGNC NCBI

Linked Data

dbSNP Id: rs1658081970
MyVariant Identifiers: chr1:g.198867681A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.198898552A>C , CM000663.2:g.198898552A>C GRCh38
NC_000001.10:g.198867681A>C , CM000663.1:g.198867681A>C GRCh37
NC_000001.9:g.197134304A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040073.1:n.363+1859T>G