Canonical Allele Identifier: CA2159147435
Gene: MIR1185-2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.101044276G= , CM000676.2:g.101044276G= GRCh38
NC_000014.8:g.101510613G= , CM000676.1:g.101510613G= GRCh37
NC_000014.7:g.100580366G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_031571.1:n.79G=