Canonical Allele Identifier: CA729929023
Gene: MIR181A1HG HGNC NCBI

Linked Data

dbSNP Id: rs1333056127
gnomAD v3: 1-198898392-T-C
gnomAD v4: 1-198898392-T-C
MyVariant Identifiers: chr1:g.198867521T>C (hg19) chr1:g.198898392T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.198898392T>C , CM000663.2:g.198898392T>C GRCh38
NC_000001.10:g.198867521T>C , CM000663.1:g.198867521T>C GRCh37
NC_000001.9:g.197134144T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040073.1:n.363+2019A>G
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