Canonical Allele Identifier: CA528537699
Gene: MIR181A1HG HGNC NCBI

Linked Data

dbSNP Id: rs1210714468
gnomAD v2: 1-198867336-C-T
MyVariant Identifiers: chr1:g.198867336C>T (hg19) chr1:g.198898207C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.198898207C>T , CM000663.2:g.198898207C>T GRCh38
NC_000001.10:g.198867336C>T , CM000663.1:g.198867336C>T GRCh37
NC_000001.9:g.197133959C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040073.1:n.363+2204G>A
Search 100 bp 5'
Search 100 bp 3'