Canonical Allele Identifier: CA2159157466
Community Standard Title: NC_000014.9:g.101056219T=
Gene: MIR323B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.101056219T= , CM000676.2:g.101056219T= GRCh38
NC_000014.8:g.101522556T= , CM000676.1:g.101522556T= GRCh37
NC_000014.7:g.100592309T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_036133.1:n.1T=