Canonical Allele Identifier: CA2548156199
Gene: LINC02268 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.174106385G>A , CM000666.2:g.174106385G>A GRCh38
NC_000004.11:g.175027536G>A , CM000666.1:g.175027536G>A GRCh37
NC_000004.10:g.175264111G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125896.1:n.276-8556C>T
XR_939484.1:n.877+18746G>A
XR_939485.1:n.877+18746G>A