Canonical Allele Identifier: CA1763972917
Gene: LINC00208 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11577984C= , CM000670.2:g.11577984C= GRCh38
NC_000008.10:g.11435493C= , CM000670.1:g.11435493C= GRCh37
NC_000008.9:g.11472902C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040035.1:n.784-386C=