Canonical Allele Identifier: CA2594558279
Gene: LINC02571 HGNC NCBI

Linked Data

dbSNP Id: rs2114020960
gnomAD v3: 6-31306643-C-A
gnomAD v4: 6-31306643-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31306643C>A , CM000668.2:g.31306643C>A GRCh38
NC_000006.11:g.31274420C>A , CM000668.1:g.31274420C>A GRCh37
NC_000006.10:g.31382399C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_926691.1:n.949+135G>T
XR_926691.2:n.965+135G>T