Canonical Allele Identifier: CA36189952
Gene: MIR181A1HG HGNC NCBI

Linked Data

dbSNP Id: rs1040152415

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.198898314A>G , CM000663.2:g.198898314A>G GRCh38
NC_000001.10:g.198867443A>G , CM000663.1:g.198867443A>G GRCh37
NC_000001.9:g.197134066A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040073.1:n.363+2097T>C