Canonical Allele Identifier: CA1763972920
Gene: LINC00208 HGNC NCBI

Linked Data

dbSNP Id: rs1802028506
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11577987A>G , CM000670.2:g.11577987A>G GRCh38
NC_000008.10:g.11435496A>G , CM000670.1:g.11435496A>G GRCh37
NC_000008.9:g.11472905A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040035.1:n.784-383A>G
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