Canonical Allele Identifier: CA1763972883
Gene: LINC00208 HGNC NCBI

Linked Data

dbSNP Id: rs1802027056

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11577922T>A , CM000670.2:g.11577922T>A GRCh38
NC_000008.10:g.11435431T>A , CM000670.1:g.11435431T>A GRCh37
NC_000008.9:g.11472840T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_040035.1:n.784-448T>A