Canonical Allele Identifier: CA2507693331
Gene: LINC02268 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.174106390T>G , CM000666.2:g.174106390T>G GRCh38
NC_000004.11:g.175027541T>G , CM000666.1:g.175027541T>G GRCh37
NC_000004.10:g.175264116T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_125896.1:n.276-8561A>C
XR_939484.1:n.877+18751T>G
XR_939485.1:n.877+18751T>G