Canonical Allele Identifier: CA136833293

Gene: LINC02571

Linked Data

• dbSNP Id: rs147161536
• gnomAD v2: 6-31274345-A-G
• gnomAD v3: 6-31306568-A-G
• gnomAD v4: 6-31306568-A-G
• MyVariant Identifiers: chr6:g.31274345A>G (hg19) ; chr6:g.31306568A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31306568A>G , CM000668.2:g.31306568A>G	GRCh38
NC_000006.11:g.31274345A>G , CM000668.1:g.31274345A>G	GRCh37
NC_000006.10:g.31382324A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_926691.1:n.949+210T>C
XR_926691.2:n.965+210T>C