Canonical Allele Identifier: CA2133363582
Gene: LINC02302 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.44637562G= , CM000676.2:g.44637562G= GRCh38
NC_000014.8:g.45106765G= , CM000676.1:g.45106765G= GRCh37
NC_000014.7:g.44176515G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943800.1:n.226-40549C=
XR_943801.1:n.226-40549C=
XR_943806.1:n.226-40549C=
XR_943808.1:n.126+160368C=