Canonical Allele Identifier: CA846003552
Gene: LINC00208 HGNC NCBI

Linked Data

dbSNP Id: rs1218232777
MyVariant Identifiers: chr8:g.11435213G>C (hg19) chr8:g.11577704G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11577704G>C , CM000670.2:g.11577704G>C GRCh38
NC_000008.10:g.11435213G>C , CM000670.1:g.11435213G>C GRCh37
NC_000008.9:g.11472622G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040035.1:n.783+387G>C
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