Canonical Allele Identifier: CA1763768665
Gene: LINC00529 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11261528C= , CM000670.2:g.11261528C= GRCh38
NC_000008.10:g.11119037C= , CM000670.1:g.11119037C= GRCh37
NC_000008.9:g.11156447C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170283.1:n.558+6261G=