Canonical Allele Identifier: CA2350037087
Gene: LINC02871 HGNC NCBI

Linked Data

dbSNP Id: rs62185668

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.10981287C>T , CM000682.2:g.10981287C>T GRCh38
NC_000020.10:g.10961935C>T , CM000682.1:g.10961935C>T GRCh37
NC_000020.9:g.10909935C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_937255.1:n.3286-10311C>T