Canonical Allele Identifier: CA2651924447
Gene: LINC00687 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

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