Canonical Allele Identifier: CA9637637
Gene: MIR521-2 HGNC NCBI

Linked Data

dbSNP Id: rs13382089

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
NR_030203.1:n.7G>T