Canonical Allele Identifier: CA1619098698
Gene: LINC02571 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31306679A= , CM000668.2:g.31306679A= GRCh38
NC_000006.11:g.31274456A= , CM000668.1:g.31274456A= GRCh37
NC_000006.10:g.31382435A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_926691.1:n.949+99T=
XR_926691.2:n.965+99T=