Canonical Allele Identifier: CA1619098545
Gene: LINC02571 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31306468A= , CM000668.2:g.31306468A= GRCh38
NC_000006.11:g.31274245A= , CM000668.1:g.31274245A= GRCh37
NC_000006.10:g.31382224A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926691.1:n.949+310T=
XR_926691.2:n.965+310T=