Canonical Allele Identifier: CA2801395362
Gene: LINC02302 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.44637389C>T , CM000676.2:g.44637389C>T GRCh38
NC_000014.8:g.45106592C>T , CM000676.1:g.45106592C>T GRCh37
NC_000014.7:g.44176342C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943800.1:n.226-40376G>A
XR_943801.1:n.226-40376G>A
XR_943806.1:n.226-40376G>A
XR_943808.1:n.126+160541G>A