Canonical Allele Identifier: CA15350945
Gene: LINC02268 HGNC NCBI

Linked Data

dbSNP Id: rs55768019

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.174106365A>G , CM000666.2:g.174106365A>G GRCh38
NC_000004.11:g.175027516A>G , CM000666.1:g.175027516A>G GRCh37
NC_000004.10:g.175264091A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_125896.1:n.276-8536T>C
XR_939484.1:n.877+18726A>G
XR_939485.1:n.877+18726A>G