Canonical Allele Identifier: CA729929052
Gene: MIR181A1HG HGNC NCBI

Linked Data

dbSNP Id: rs1379011533
MyVariant Identifiers: chr1:g.198867586A>G (hg19) chr1:g.198898457A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.198898457A>G , CM000663.2:g.198898457A>G GRCh38
NC_000001.10:g.198867586A>G , CM000663.1:g.198867586A>G GRCh37
NC_000001.9:g.197134209A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040073.1:n.363+1954T>C
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