Canonical Allele Identifier: CA1514142861
Gene: LINC02268 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.174106383T= , CM000666.2:g.174106383T= GRCh38
NC_000004.11:g.175027534T= , CM000666.1:g.175027534T= GRCh37
NC_000004.10:g.175264109T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125896.1:n.276-8554A=
XR_939484.1:n.877+18744T=
XR_939485.1:n.877+18744T=