Canonical Allele Identifier: CA136833319

Gene: LINC02571

Linked Data

• dbSNP Id: rs975357223
• MyVariant Identifiers: chr6:g.31274406C>T (hg19) ; chr6:g.31306629C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31306629C>T , CM000668.2:g.31306629C>T	GRCh38
NC_000006.11:g.31274406C>T , CM000668.1:g.31274406C>T	GRCh37
NC_000006.10:g.31382385C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_926691.1:n.949+149G>A
XR_926691.2:n.965+149G>A