Canonical Allele Identifier: CA823867002
Gene: LINC02571 HGNC NCBI

Linked Data

dbSNP Id: rs1304325309

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31306608A>T , CM000668.2:g.31306608A>T GRCh38
NC_000006.11:g.31274385A>T , CM000668.1:g.31274385A>T GRCh37
NC_000006.10:g.31382364A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_926691.1:n.949+170T>A
XR_926691.2:n.965+170T>A