Canonical Allele Identifier: CA1619098679
Gene: LINC02571 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31306655T= , CM000668.2:g.31306655T= GRCh38
NC_000006.11:g.31274432T= , CM000668.1:g.31274432T= GRCh37
NC_000006.10:g.31382411T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_926691.1:n.949+123A=
XR_926691.2:n.965+123A=