How can I locate exon or intron number (and genomic position) from known mutation positions using HGVS nomenclature?

For example, how to determine the exon/intron location from 711+1G>T mutation - CFTR (cystic fibrosis) human gene? I'm confused whether I have to use the nucleotide numbering from coding or...

09 September 2015 6,228 5 View