Canonical Allele Identifier: CA11668719
Gene: LINC02268 HGNC NCBI

Linked Data

dbSNP Id: rs56286907

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.174106286C>T , CM000666.2:g.174106286C>T GRCh38
NC_000004.11:g.175027437C>T , CM000666.1:g.175027437C>T GRCh37
NC_000004.10:g.175264012C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125896.1:n.276-8457G>A
XR_939484.1:n.877+18647C>T
XR_939485.1:n.877+18647C>T