Canonical Allele Identifier: CA566338525

Gene: LINC02571

Linked Data

• dbSNP Id: rs9264941
• gnomAD v2: 6-31274298-G-C
• gnomAD v3: 6-31306521-G-C
• gnomAD v4: 6-31306521-G-C
• MyVariant Identifiers: chr6:g.31274298G>C (hg19) ; chr6:g.31306521G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31306521G>C , CM000668.2:g.31306521G>C	GRCh38
NC_000006.11:g.31274298G>C , CM000668.1:g.31274298G>C	GRCh37
NC_000006.10:g.31382277G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_926691.1:n.949+257C>G
XR_926691.2:n.965+257C>G