Canonical Allele Identifier: CA1763972869
Gene: LINC00208 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11577899A= , CM000670.2:g.11577899A= GRCh38
NC_000008.10:g.11435408A= , CM000670.1:g.11435408A= GRCh37
NC_000008.9:g.11472817A= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_040035.1:n.784-471A=