Canonical Allele Identifier: CA311933743
Gene: LINC00687 HGNC NCBI

Linked Data

dbSNP Id: rs1136200

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.11810038G>T , CM000682.2:g.11810038G>T GRCh38
NC_000020.10:g.11790686G>T , CM000682.1:g.11790686G>T GRCh37
NC_000020.9:g.11738686G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110635.1:n.473C>A