Canonical Allele Identifier: CA172383962
Gene: LINC00208 HGNC NCBI

Linked Data

dbSNP Id: rs751482774
MyVariant Identifiers: chr8:g.11577886C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11577886C>A , CM000670.2:g.11577886C>A GRCh38
NC_000008.10:g.11435395C>A , CM000670.1:g.11435395C>A GRCh37
NC_000008.9:g.11472804C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040035.1:n.784-484C>A
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