Canonical Allele Identifier: CA2581561871
Gene: LINC02571 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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