Canonical Allele Identifier: CA729929032
Gene: MIR181A1HG HGNC NCBI

Linked Data

dbSNP Id: rs1334012142
gnomAD v4: 1-198898410-T-C
MyVariant Identifiers: chr1:g.198867539T>C (hg19) chr1:g.198898410T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.198898410T>C , CM000663.2:g.198898410T>C GRCh38
NC_000001.10:g.198867539T>C , CM000663.1:g.198867539T>C GRCh37
NC_000001.9:g.197134162T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040073.1:n.363+2001A>G
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