Canonical Allele Identifier: CA136833341

Gene: LINC02571

Linked Data

• dbSNP Id: rs1003221356
• gnomAD v2: 6-31274456-A-T
• gnomAD v3: 6-31306679-A-T
• gnomAD v4: 6-31306679-A-T
• MyVariant Identifiers: chr6:g.31274456A>T (hg19) ; chr6:g.31306679A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31306679A>T , CM000668.2:g.31306679A>T	GRCh38
NC_000006.11:g.31274456A>T , CM000668.1:g.31274456A>T	GRCh37
NC_000006.10:g.31382435A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_926691.1:n.949+99T>A
XR_926691.2:n.965+99T>A