Canonical Allele Identifier: CA2140086902
Gene: LINC01500 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.58867432_58867433delinsCT , CM000676.2:g.58867432_58867433delinsCT GRCh38
NC_000014.8:g.59334150_59334151delinsCT , CM000676.1:g.59334150_59334151delinsCT GRCh37
NC_000014.7:g.58403903_58403904delinsCT NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110547.1:n.269-26711_269-26710delinsCT
Search 100 bp 5'
Search 100 bp 3'