Canonical Allele Identifier: CA2779060969
Gene: LINC00208 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11577854G>C , CM000670.2:g.11577854G>C GRCh38
NC_000008.10:g.11435363G>C , CM000670.1:g.11435363G>C GRCh37
NC_000008.9:g.11472772G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040035.1:n.784-516G>C