Canonical Allele Identifier: CA2779060974
Gene: LINC00208 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11577968G>T , CM000670.2:g.11577968G>T GRCh38
NC_000008.10:g.11435477G>T , CM000670.1:g.11435477G>T GRCh37
NC_000008.9:g.11472886G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040035.1:n.784-402G>T
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