Figure 1.

Mapping of variants onto alternative transcripts. Submitted variant descriptions are automatically mapped, via the selected genome build (GRCh38), onto all other transcripts that overlap the same genomic position. In this example, NM_182763.2:c.688+403C>T, which is intronic with respect to MCL1 transcript variant 2 mRNA, is mapped to an exonic variant in MCL1 transcript variant 1 mRNA, NM_021960.4:c.740C>T. The same initial variant description also maps to an exonic variant in MCL1 transcript variant 3 mRNA, NM_001197320.1:c.281C>T