HGVS | Genome Assembly |
---|---|
NC_000011.10:g.117317472A>G , CM000673.2:g.117317472A>G | GRCh38 |
NC_000011.9:g.117188188A>G , CM000673.1:g.117188188A>G | GRCh37 |
NC_000011.8:g.116693398A>G | NCBI36 |
NG_029372.1:g.3785T>C | |
NG_033032.1:g.695A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000525734.5:c.-98+2744A>G | ENSP00000436609.1:n.-98+2744A>G | |
XM_017017364.1:c.-98+939A>G | XP_016872853.1:n.-98+939A>G |