Canonical Allele Identifier: CA1619098579
Gene: LINC02571 HGNC NCBI

Linked Data

dbSNP Id: rs1763431082

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31306518C>T , CM000668.2:g.31306518C>T GRCh38
NC_000006.11:g.31274295C>T , CM000668.1:g.31274295C>T GRCh37
NC_000006.10:g.31382274C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_926691.1:n.949+260G>A
XR_926691.2:n.965+260G>A