Canonical Allele Identifier: CA2148220476
Gene: LINC02288 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.77047501T>A , CM000676.2:g.77047501T>A GRCh38
NC_000014.8:g.77513844T>A , CM000676.1:g.77513844T>A GRCh37
NC_000014.7:g.76583597T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110554.1:n.229+6224T>A