Canonical Allele Identifier: CA1071107313
Gene: LINC02268 HGNC NCBI

Linked Data

dbSNP Id: rs1732971579

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.174106281T>C , CM000666.2:g.174106281T>C GRCh38
NC_000004.11:g.175027432T>C , CM000666.1:g.175027432T>C GRCh37
NC_000004.10:g.175264007T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125896.1:n.276-8452A>G
XR_939484.1:n.877+18642T>C
XR_939485.1:n.877+18642T>C