Canonical Allele Identifier: CA1619098481
Gene: LINC02571 HGNC NCBI

Linked Data

dbSNP Id: rs1763419760

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31306410del , CM000668.2:g.31306410del GRCh38
NC_000006.11:g.31274187del , CM000668.1:g.31274187del GRCh37
NC_000006.10:g.31382166del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_926691.1:n.949+368del
XR_926691.2:n.965+368del