Canonical Allele Identifier: CA1619098683
Gene: LINC02571 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31306663C= , CM000668.2:g.31306663C= GRCh38
NC_000006.11:g.31274440C= , CM000668.1:g.31274440C= GRCh37
NC_000006.10:g.31382419C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_926691.1:n.949+115G=
XR_926691.2:n.965+115G=