HGVS | Genome Assembly |
---|---|
NC_000001.11:g.179575975A>C , CM000663.2:g.179575975A>C | GRCh38 |
NC_000001.10:g.179545110A>C , CM000663.1:g.179545110A>C | GRCh37 |
NC_000001.9:g.177811733A>C | NCBI36 |
NG_007535.1:g.4975T>G , LRG_887:g.4975T>G |
HGVS | Amino-acid Change | |
---|---|---|
XM_006711529.2:c.-111T>G | XP_006711592.1:n.-111T>G | |
XM_017002298.1:c.-111T>G | XP_016857787.1:n.-111T>G | |
XM_017002299.1:c.-111T>G | XP_016857788.1:n.-111T>G |