Deanna Church

GRCh38 splign alignments available?

6

Hi- I'm doing some variant mapping. Starting with this: ``` v = hp.parse_hgvs_variant("NM_007194.4(CHEK2):c.1611T>A") print(v) print(v.posedit.pos.start) print(v.posedit.edit.ref) ``` I get: NM_007194.4(CHEK2):c.1611T>A 1611 T All is good. I can get the genomic...