Canonical Allele Identifier: CA2349984566
Gene: LINC02871 HGNC NCBI

Linked Data

dbSNP Id: rs1984548396

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.10869745A>G , CM000682.2:g.10869745A>G GRCh38
NC_000020.10:g.10850393A>G , CM000682.1:g.10850393A>G GRCh37
NC_000020.9:g.10798393A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_937255.1:n.2829+2438A>G