Canonical Allele Identifier: CA1763972952
Gene: LINC00208 HGNC NCBI

Linked Data

dbSNP Id: rs1802029827

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11578050G>C , CM000670.2:g.11578050G>C GRCh38
NC_000008.10:g.11435559G>C , CM000670.1:g.11435559G>C GRCh37
NC_000008.9:g.11472968G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_040035.1:n.784-320G>C