Canonical Allele Identifier: CA528537708
Gene: MIR181A1HG HGNC NCBI

Linked Data

dbSNP Id: rs1307775129
gnomAD v2: 1-198867541-C-T
gnomAD v3: 1-198898412-C-T
gnomAD v4: 1-198898412-C-T
MyVariant Identifiers: chr1:g.198867541C>T (hg19) chr1:g.198898412C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.198898412C>T , CM000663.2:g.198898412C>T GRCh38
NC_000001.10:g.198867541C>T , CM000663.1:g.198867541C>T GRCh37
NC_000001.9:g.197134164C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040073.1:n.363+1999G>A
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