Canonical Allele Identifier: CA2580582048
Gene: LINC02571 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31306603T>A , CM000668.2:g.31306603T>A GRCh38
NC_000006.11:g.31274380T>A , CM000668.1:g.31274380T>A GRCh37
NC_000006.10:g.31382359T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_926691.1:n.949+175A>T
XR_926691.2:n.965+175A>T