Canonical Allele Identifier: CA136833268
Gene: LINC02571 HGNC NCBI

Linked Data

dbSNP Id: rs386699022

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31306490_31306492delinsGTA , CM000668.2:g.31306490_31306492delinsGTA GRCh38
NC_000006.11:g.31274267_31274269delinsGTA , CM000668.1:g.31274267_31274269delinsGTA GRCh37
NC_000006.10:g.31382246_31382248delinsGTA NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_926691.1:n.949+286_949+288delinsTAC
XR_926691.2:n.965+286_965+288delinsTAC