Canonical Allele Identifier: CA1619098661
Gene: LINC02571 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31306613G= , CM000668.2:g.31306613G= GRCh38
NC_000006.11:g.31274390G= , CM000668.1:g.31274390G= GRCh37
NC_000006.10:g.31382369G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_926691.1:n.949+165C=
XR_926691.2:n.965+165C=