Canonical Allele Identifier: CA2272849647
Gene: LINC01483 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.69854627_69854629delinsCAA , CM000679.2:g.69854627_69854629delinsCAA GRCh38
NC_000017.10:g.67850768_67850770delinsCAA , CM000679.1:g.67850768_67850770delinsCAA GRCh37
NC_000017.9:g.65362363_65362365delinsCAA NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109971.1:n.363+9141_363+9143delinsCAA
NR_109972.1:n.363+9141_363+9143delinsCAA
Search 100 bp 5'
Search 100 bp 3'