Canonical Allele Identifier: CA36189959
Gene: MIR181A1HG HGNC NCBI

Linked Data

dbSNP Id: rs186231394
gnomAD v2: 1-198867518-G-T
gnomAD v3: 1-198898389-G-T
gnomAD v4: 1-198898389-G-T
MyVariant Identifiers: chr1:g.198867518G>T (hg19) chr1:g.198898389G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.198898389G>T , CM000663.2:g.198898389G>T GRCh38
NC_000001.10:g.198867518G>T , CM000663.1:g.198867518G>T GRCh37
NC_000001.9:g.197134141G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040073.1:n.363+2022C>A
Search 100 bp 5'
Search 100 bp 3'