Canonical Allele Identifier: CA1619098625
Gene: LINC02571 HGNC NCBI

Linked Data

dbSNP Id: rs1763435632

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31306592G>A , CM000668.2:g.31306592G>A GRCh38
NC_000006.11:g.31274369G>A , CM000668.1:g.31274369G>A GRCh37
NC_000006.10:g.31382348G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_926691.1:n.949+186C>T
XR_926691.2:n.965+186C>T