Canonical Allele Identifier: CA1110700046
Gene: LINC00208 HGNC NCBI

Linked Data

dbSNP Id: rs1802025732
gnomAD v3: 8-11577872-C-A
gnomAD v4: 8-11577872-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11577872C>A , CM000670.2:g.11577872C>A GRCh38
NC_000008.10:g.11435381C>A , CM000670.1:g.11435381C>A GRCh37
NC_000008.9:g.11472790C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040035.1:n.784-498C>A
Search 100 bp 5'
Search 100 bp 3'