Canonical Allele Identifier: CA2342483934
Gene: MIR521-2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53716600G= , CM000681.2:g.53716600G= GRCh38
NC_000019.9:g.54219854G= , CM000681.1:g.54219854G= GRCh37
NC_000019.8:g.58911666G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_030203.1:n.7G=