Canonical Allele Identifier: CA1087445546
Gene: LINC02571 HGNC NCBI

Linked Data

dbSNP Id: rs1763424193
gnomAD v3: 6-31306450-G-A
gnomAD v4: 6-31306450-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31306450G>A , CM000668.2:g.31306450G>A GRCh38
NC_000006.11:g.31274227G>A , CM000668.1:g.31274227G>A GRCh37
NC_000006.10:g.31382206G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926691.1:n.949+328C>T
XR_926691.2:n.965+328C>T