Canonical Allele Identifier: CA1889430968
Gene: LINC02676 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.8912261A= , CM000672.2:g.8912261A= GRCh38
NC_000010.10:g.8954224A= , CM000672.1:g.8954224A= GRCh37
NC_000010.9:g.8994230A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_131944.1:n.176-1561A=
XR_930641.1:n.32+153102T=