Canonical Allele Identifier: CA566338528
Gene: LINC02571 HGNC NCBI

Linked Data

dbSNP Id: rs1562082667

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31306604_31306608del , CM000668.2:g.31306604_31306608del GRCh38
NC_000006.11:g.31274381_31274385del , CM000668.1:g.31274381_31274385del GRCh37
NC_000006.10:g.31382360_31382364del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_926691.1:n.949+170_949+174del
XR_926691.2:n.965+170_965+174del