Canonical Allele Identifier: CA1619098569
Gene: LINC02571 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31306501T= , CM000668.2:g.31306501T= GRCh38
NC_000006.11:g.31274278T= , CM000668.1:g.31274278T= GRCh37
NC_000006.10:g.31382257T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_926691.1:n.949+277A=
XR_926691.2:n.965+277A=