Canonical Allele Identifier: CA1619098591
Gene: LINC02571 HGNC NCBI

Linked Data

dbSNP Id: rs1763432401

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31306530_31306534del , CM000668.2:g.31306530_31306534del GRCh38
NC_000006.11:g.31274307_31274311del , CM000668.1:g.31274307_31274311del GRCh37
NC_000006.10:g.31382286_31382290del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_926691.1:n.949+245_949+249del
XR_926691.2:n.965+245_965+249del