Canonical Allele Identifier: CA1763972841
Gene: LINC00208 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11577833T= , CM000670.2:g.11577833T= GRCh38
NC_000008.10:g.11435342T= , CM000670.1:g.11435342T= GRCh37
NC_000008.9:g.11472751T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040035.1:n.783+516T=