Canonical Allele Identifier: CA2350433821
Gene: LINC00687 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.11810033T= , CM000682.2:g.11810033T= GRCh38
NC_000020.10:g.11790681T= , CM000682.1:g.11790681T= GRCh37
NC_000020.9:g.11738681T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110635.1:n.478A=