Canonical Allele Identifier: CA422742988
Gene: MIR181A1HG HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.198867610T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.198898481T>A , CM000663.2:g.198898481T>A GRCh38
NC_000001.10:g.198867610T>A , CM000663.1:g.198867610T>A GRCh37
NC_000001.9:g.197134233T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040073.1:n.363+1930A>T
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