Canonical Allele Identifier: CA1619098531
Gene: LINC02571 HGNC NCBI

Linked Data

dbSNP Id: rs1763425364

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31306471_31306472dup , CM000668.2:g.31306471_31306472dup GRCh38
NC_000006.11:g.31274248_31274249dup , CM000668.1:g.31274248_31274249dup GRCh37
NC_000006.10:g.31382227_31382228dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926691.1:n.949+315_949+316dup
XR_926691.2:n.965+315_965+316dup