Canonical Allele Identifier: CA1763972815
Gene: LINC00208 HGNC NCBI

Linked Data

dbSNP Id: rs1802023240
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11577786C>G , CM000670.2:g.11577786C>G GRCh38
NC_000008.10:g.11435295C>G , CM000670.1:g.11435295C>G GRCh37
NC_000008.9:g.11472704C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040035.1:n.783+469C>G
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