Canonical Allele Identifier: CA1763972911
Gene: LINC00208 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11577969A= , CM000670.2:g.11577969A= GRCh38
NC_000008.10:g.11435478A= , CM000670.1:g.11435478A= GRCh37
NC_000008.9:g.11472887A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040035.1:n.784-401A=