Canonical Allele Identifier: CA823867001

Gene: LINC02571

Linked Data

• dbSNP Id: rs1306780206
• gnomAD v3: 6-31306583-C-T
• gnomAD v4: 6-31306583-C-T
• MyVariant Identifiers: chr6:g.31274360C>T (hg19) ; chr6:g.31306583C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31306583C>T , CM000668.2:g.31306583C>T	GRCh38
NC_000006.11:g.31274360C>T , CM000668.1:g.31274360C>T	GRCh37
NC_000006.10:g.31382339C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_926691.1:n.949+195G>A
XR_926691.2:n.965+195G>A