Canonical Allele Identifier: CA11963850
Gene: LINC02211 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.25419980G>A , CM000667.2:g.25419980G>A GRCh38
NC_000005.9:g.25420089G>A , CM000667.1:g.25420089G>A GRCh37
NC_000005.8:g.25455846G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011514196.1:c.*59+63882G>A XP_011512498.1:n.*59+63882G>A
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