Canonical Allele Identifier: CA1619098668
Gene: LINC02571 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31306639T= , CM000668.2:g.31306639T= GRCh38
NC_000006.11:g.31274416T= , CM000668.1:g.31274416T= GRCh37
NC_000006.10:g.31382395T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_926691.1:n.949+139A=
XR_926691.2:n.965+139A=