Canonical Allele Identifier: CA2581561875
Gene: LINC02571 HGNC NCBI

Linked Data

dbSNP Id: rs9264936
gnomAD v3: 6-31306480-G-A
gnomAD v4: 6-31306480-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31306480G>A , CM000668.2:g.31306480G>A GRCh38
NC_000006.11:g.31274257G>A , CM000668.1:g.31274257G>A GRCh37
NC_000006.10:g.31382236G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926691.1:n.949+298C>T
XR_926691.2:n.965+298C>T