Canonical Allele Identifier: CA1619098553
Gene: LINC02571 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31306477A= , CM000668.2:g.31306477A= GRCh38
NC_000006.11:g.31274254A= , CM000668.1:g.31274254A= GRCh37
NC_000006.10:g.31382233A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926691.1:n.949+301T=
XR_926691.2:n.965+301T=