Canonical Allele Identifier: CA2349984585
Gene: LINC02871 HGNC NCBI

Linked Data

dbSNP Id: rs1984548783

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.10869791T>C , CM000682.2:g.10869791T>C GRCh38
NC_000020.10:g.10850439T>C , CM000682.1:g.10850439T>C GRCh37
NC_000020.9:g.10798439T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_937255.1:n.2829+2484T>C