Canonical Allele Identifier: CA1619098502
Gene: LINC02571 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31306429T= , CM000668.2:g.31306429T= GRCh38
NC_000006.11:g.31274206T= , CM000668.1:g.31274206T= GRCh37
NC_000006.10:g.31382185T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_926691.1:n.949+349A=
XR_926691.2:n.965+349A=