Canonical Allele Identifier: CA566338529

Gene: LINC02571

Linked Data

• dbSNP Id: rs1467525514
• gnomAD v2: 6-31274397-T-C
• gnomAD v3: 6-31306620-T-C
• gnomAD v4: 6-31306620-T-C
• MyVariant Identifiers: chr6:g.31274397T>C (hg19) ; chr6:g.31306620T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31306620T>C , CM000668.2:g.31306620T>C	GRCh38
NC_000006.11:g.31274397T>C , CM000668.1:g.31274397T>C	GRCh37
NC_000006.10:g.31382376T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_926691.1:n.949+158A>G
XR_926691.2:n.965+158A>G