Canonical Allele Identifier: CA823866998

Gene: LINC02571

Linked Data

• dbSNP Id: rs1487912355
• gnomAD v3: 6-31306558-G-A
• gnomAD v4: 6-31306558-G-A
• MyVariant Identifiers: chr6:g.31274335G>A (hg19) ; chr6:g.31306558G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31306558G>A , CM000668.2:g.31306558G>A	GRCh38
NC_000006.11:g.31274335G>A , CM000668.1:g.31274335G>A	GRCh37
NC_000006.10:g.31382314G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_926691.1:n.949+220C>T
XR_926691.2:n.965+220C>T