Canonical Allele Identifier: CA1763972899
Gene: LINC00208 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11577937G= , CM000670.2:g.11577937G= GRCh38
NC_000008.10:g.11435446G= , CM000670.1:g.11435446G= GRCh37
NC_000008.9:g.11472855G= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_040035.1:n.784-433G=