Canonical Allele Identifier: CA1619098602
Gene: LINC02571 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31306555A= , CM000668.2:g.31306555A= GRCh38
NC_000006.11:g.31274332A= , CM000668.1:g.31274332A= GRCh37
NC_000006.10:g.31382311A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_926691.1:n.949+223T=
XR_926691.2:n.965+223T=