Canonical Allele Identifier: CA422742986
Gene: MIR181A1HG HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.198867609C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.198898480C>T , CM000663.2:g.198898480C>T GRCh38
NC_000001.10:g.198867609C>T , CM000663.1:g.198867609C>T GRCh37
NC_000001.9:g.197134232C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040073.1:n.363+1931G>A
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