Canonical Allele Identifier: CA36189939
Gene: MIR181A1HG HGNC NCBI

Linked Data

dbSNP Id: rs746286781
gnomAD v3: 1-198898192-A-C
gnomAD v4: 1-198898192-A-C
MyVariant Identifiers: chr1:g.198867321A>C (hg19) chr1:g.198898192A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.198898192A>C , CM000663.2:g.198898192A>C GRCh38
NC_000001.10:g.198867321A>C , CM000663.1:g.198867321A>C GRCh37
NC_000001.9:g.197133944A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040073.1:n.363+2219T>G
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