Canonical Allele Identifier: CA1763972897
Gene: LINC00208 HGNC NCBI

Linked Data

dbSNP Id: rs1802027499
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11577934A>T , CM000670.2:g.11577934A>T GRCh38
NC_000008.10:g.11435443A>T , CM000670.1:g.11435443A>T GRCh37
NC_000008.9:g.11472852A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040035.1:n.784-436A>T
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Search 100 bp 3'