Canonical Allele Identifier: CA1619098529
Gene: LINC02571 HGNC NCBI

Linked Data

dbSNP Id: rs1763425364

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31306469_31306472del , CM000668.2:g.31306469_31306472del GRCh38
NC_000006.11:g.31274246_31274249del , CM000668.1:g.31274246_31274249del GRCh37
NC_000006.10:g.31382225_31382228del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926691.1:n.949+313_949+316del
XR_926691.2:n.965+313_965+316del