Canonical Allele Identifier: CA823867003

Gene: LINC02571

Linked Data

• dbSNP Id: rs1290783177
• MyVariant Identifiers: chr6:g.31274428C>T (hg19) ; chr6:g.31306651C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31306651C>T , CM000668.2:g.31306651C>T	GRCh38
NC_000006.11:g.31274428C>T , CM000668.1:g.31274428C>T	GRCh37
NC_000006.10:g.31382407C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_926691.1:n.949+127G>A
XR_926691.2:n.965+127G>A