Thanks for the reply :).
- the name of the chromosome might change 1 vs chr1
True, but this will not happen within one analysis, where you mostly stick to the same genome/annotation
- you should add the build grch37:1:1234:A:T
The argument from the above point also counts for here I think. For cross genome uniqueness that would be a good idea.
- there's symbolic alleles : chr1:77:A:<DELETION>
Does this happen often. Isn't a deletion normally shown by fewer ALT then REF bases?
- multiallelic variants: chr1:777:A:T,C
Also true, but I almost always split them.
- normalization : chr1:10:A:ATT vs chr1:10:AA:AAT
This point I don't get. Could you elaborate this?
if both the build and the nomenclature system are promulgated