Canonical Allele Identifier: CA13948923
Gene: LINC02325 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.97521520G>A , CM000676.2:g.97521520G>A GRCh38
NC_000014.8:g.97987857G>A , CM000676.1:g.97987857G>A GRCh37
NC_000014.7:g.97057610G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110166.1:n.223+11155G>A