Canonical Allele Identifier: CA2150809738
Gene: LINC02301 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.82739726A= , CM000676.2:g.82739726A= GRCh38
NC_000014.8:g.83206070A= , CM000676.1:g.83206070A= GRCh37
NC_000014.7:g.82275823A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_944088.1:n.362-973A=