Canonical Allele Identifier: CA136833322

Gene: LINC02571

Linked Data

• dbSNP Id: rs780006220
• MyVariant Identifiers: chr6:g.31274418C>A (hg19) ; chr6:g.31306641C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31306641C>A , CM000668.2:g.31306641C>A	GRCh38
NC_000006.11:g.31274418C>A , CM000668.1:g.31274418C>A	GRCh37
NC_000006.10:g.31382397C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_926691.1:n.949+137G>T
XR_926691.2:n.965+137G>T