Canonical Allele Identifier: CA1619098662
Gene: LINC02571 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31306620T= , CM000668.2:g.31306620T= GRCh38
NC_000006.11:g.31274397T= , CM000668.1:g.31274397T= GRCh37
NC_000006.10:g.31382376T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_926691.1:n.949+158A=
XR_926691.2:n.965+158A=