Canonical Allele Identifier: CA1763972856
Gene: LINC00208 HGNC NCBI

Linked Data

dbSNP Id: rs1802025797

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11577873C>T , CM000670.2:g.11577873C>T GRCh38
NC_000008.10:g.11435382C>T , CM000670.1:g.11435382C>T GRCh37
NC_000008.9:g.11472791C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040035.1:n.784-497C>T