Canonical Allele Identifier: CA12385996

Gene: LINC02571

Linked Data

• dbSNP Id: rs35647108
• gnomAD v2: 6-31274449-C-A
• gnomAD v3: 6-31306672-C-A
• gnomAD v4: 6-31306672-C-A
• MyVariant Identifiers: chr6:g.31274449C>A (hg19) ; chr6:g.31306672C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31306672C>A , CM000668.2:g.31306672C>A	GRCh38
NC_000006.11:g.31274449C>A , CM000668.1:g.31274449C>A	GRCh37
NC_000006.10:g.31382428C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_926691.1:n.949+106G>T
XR_926691.2:n.965+106G>T