Canonical Allele Identifier: CA1763972904
Gene: LINC00208 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11577945T= , CM000670.2:g.11577945T= GRCh38
NC_000008.10:g.11435454T= , CM000670.1:g.11435454T= GRCh37
NC_000008.9:g.11472863T= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_040035.1:n.784-425T=