Canonical Allele Identifier: CA422742907
Gene: MIR181A1HG HGNC NCBI

Linked Data

dbSNP Id: rs1658080587
MyVariant Identifiers: chr1:g.198867597T>A (hg19)

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