Canonical Allele Identifier: CA1087445561
Gene: LINC02571 HGNC NCBI

Linked Data

dbSNP Id: rs1763429182
gnomAD v3: 6-31306496-T-G
gnomAD v4: 6-31306496-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31306496T>G , CM000668.2:g.31306496T>G GRCh38
NC_000006.11:g.31274273T>G , CM000668.1:g.31274273T>G GRCh37
NC_000006.10:g.31382252T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_926691.1:n.949+282A>C
XR_926691.2:n.965+282A>C