Canonical Allele Identifier: CA2716438215
Gene: LINC00208 HGNC NCBI

Linked Data

dbSNP Id: rs1802021433

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11577725C>T , CM000670.2:g.11577725C>T GRCh38
NC_000008.10:g.11435234C>T , CM000670.1:g.11435234C>T GRCh37
NC_000008.9:g.11472643C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040035.1:n.783+408C>T