Canonical Allele Identifier: CA2133363551
Gene: LINC02302 HGNC NCBI

Linked Data

dbSNP Id: rs1883838635

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.44637483G>A , CM000676.2:g.44637483G>A GRCh38
NC_000014.8:g.45106686G>A , CM000676.1:g.45106686G>A GRCh37
NC_000014.7:g.44176436G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943800.1:n.226-40470C>T
XR_943801.1:n.226-40470C>T
XR_943806.1:n.226-40470C>T
XR_943808.1:n.126+160447C>T