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