Canonical Allele Identifier: CA2538862930
Gene: LINC02302 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.44637498C>A , CM000676.2:g.44637498C>A GRCh38
NC_000014.8:g.45106701C>A , CM000676.1:g.45106701C>A GRCh37
NC_000014.7:g.44176451C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943800.1:n.226-40485G>T
XR_943801.1:n.226-40485G>T
XR_943806.1:n.226-40485G>T
XR_943808.1:n.126+160432G>T