Canonical Allele Identifier: CA2651924446
Gene: LINC00687 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.11810067del , CM000682.2:g.11810067del GRCh38
NC_000020.10:g.11790715del , CM000682.1:g.11790715del GRCh37
NC_000020.9:g.11738715del NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110635.1:n.446del