Canonical Allele Identifier: CA2589856264
Gene: LINC02871 HGNC NCBI

Linked Data

dbSNP Id: rs560551841

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.10869765A>C , CM000682.2:g.10869765A>C GRCh38
NC_000020.10:g.10850413A>C , CM000682.1:g.10850413A>C GRCh37
NC_000020.9:g.10798413A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_937255.1:n.2829+2458A>C