Canonical Allele Identifier: CA1763972761
Gene: LINC00208 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11577697G= , CM000670.2:g.11577697G= GRCh38
NC_000008.10:g.11435206G= , CM000670.1:g.11435206G= GRCh37
NC_000008.9:g.11472615G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040035.1:n.783+380G=