Canonical Allele Identifier: CA1514142882

Gene: LINC02268

Linked Data

• dbSNP Id: rs1732973725

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.174106418G>A , CM000666.2:g.174106418G>A	GRCh38
NC_000004.11:g.175027569G>A , CM000666.1:g.175027569G>A	GRCh37
NC_000004.10:g.175264144G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_125896.1:n.276-8589C>T
XR_939484.1:n.877+18779G>A
XR_939485.1:n.877+18779G>A