Canonical Allele Identifier: CA2350433832
Gene: LINC00687 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.11810047G= , CM000682.2:g.11810047G= GRCh38
NC_000020.10:g.11790695G= , CM000682.1:g.11790695G= GRCh37
NC_000020.9:g.11738695G= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110635.1:n.464C=