Canonical Allele Identifier: CA2350433841
Gene: LINC00687 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.11810065A= , CM000682.2:g.11810065A= GRCh38
NC_000020.10:g.11790713A= , CM000682.1:g.11790713A= GRCh37
NC_000020.9:g.11738713A= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110635.1:n.446T=