Canonical Allele Identifier: CA2529376667
Gene: LINC02871 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.10869735T>C , CM000682.2:g.10869735T>C GRCh38
NC_000020.10:g.10850383T>C , CM000682.1:g.10850383T>C GRCh37
NC_000020.9:g.10798383T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_937255.1:n.2829+2428T>C