Canonical Allele Identifier: CA1514142879
Gene: LINC02268 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.174106414A= , CM000666.2:g.174106414A= GRCh38
NC_000004.11:g.175027565A= , CM000666.1:g.175027565A= GRCh37
NC_000004.10:g.175264140A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125896.1:n.276-8585T=
XR_939484.1:n.877+18775A=
XR_939485.1:n.877+18775A=