Canonical Allele Identifier: CA2133363529
Gene: LINC02302 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.44637438G= , CM000676.2:g.44637438G= GRCh38
NC_000014.8:g.45106641G= , CM000676.1:g.45106641G= GRCh37
NC_000014.7:g.44176391G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943800.1:n.226-40425C=
XR_943801.1:n.226-40425C=
XR_943806.1:n.226-40425C=
XR_943808.1:n.126+160492C=