Canonical Allele Identifier: CA2131574415
Gene: LINC02315 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.41054257A= , CM000676.2:g.41054257A= GRCh38
NC_000014.8:g.41523462A= , CM000676.1:g.41523462A= GRCh37
NC_000014.7:g.40593212A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109758.1:n.346+79867A=