Canonical Allele Identifier: CA1763972892
Gene: LINC00208 HGNC NCBI

Linked Data

dbSNP Id: rs1802027400

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11577932dup , CM000670.2:g.11577932dup GRCh38
NC_000008.10:g.11435441dup , CM000670.1:g.11435441dup GRCh37
NC_000008.9:g.11472850dup NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_040035.1:n.784-438dup