Canonical Allele Identifier: CA2349984561
Gene: LINC02871 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.10869732A= , CM000682.2:g.10869732A= GRCh38
NC_000020.10:g.10850380A= , CM000682.1:g.10850380A= GRCh37
NC_000020.9:g.10798380A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_937255.1:n.2829+2425A=