HGVS | Genome Assembly |
---|---|
NC_000012.12:g.75670748T>C , CM000674.2:g.75670748T>C | GRCh38 |
NC_000012.11:g.76064528T>C , CM000674.1:g.76064528T>C | GRCh37 |
NC_000012.10:g.74350795T>C | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
XR_945107.1:n.452-6942A>G | ||
XR_001749214.2:n.2193-6942A>G | ||
XR_002957419.1:n.2441-6942A>G |