Canonical Allele Identifier: CA36189936
Gene: MIR181A1HG HGNC NCBI

Linked Data

dbSNP Id: rs367590357
gnomAD v2: 1-198867305-T-G
gnomAD v3: 1-198898176-T-G
gnomAD v4: 1-198898176-T-G
MyVariant Identifiers: chr1:g.198867305T>G (hg19) chr1:g.198898176T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.198898176T>G , CM000663.2:g.198898176T>G GRCh38
NC_000001.10:g.198867305T>G , CM000663.1:g.198867305T>G GRCh37
NC_000001.9:g.197133928T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040073.1:n.363+2235A>C
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