Canonical Allele Identifier: CA1763972902
Gene: LINC00208 HGNC NCBI

Linked Data

dbSNP Id: rs1802027695

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11577943C>G , CM000670.2:g.11577943C>G GRCh38
NC_000008.10:g.11435452C>G , CM000670.1:g.11435452C>G GRCh37
NC_000008.9:g.11472861C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_040035.1:n.784-427C>G