HGVS | Genome Assembly |
---|---|
NC_000001.11:g.179575950G>T , CM000663.2:g.179575950G>T | GRCh38 |
NC_000001.10:g.179545085G>T , CM000663.1:g.179545085G>T | GRCh37 |
NC_000001.9:g.177811708G>T | NCBI36 |
NG_007535.1:g.5000C>A , LRG_887:g.5000C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367616.4:c.-86C>A | ENSP00000356588.4:n.-86C>A | |
NM_001297575.1:c.-86C>A | NP_001284504.1:n.-86C>A | |
NM_014625.3:c.-86C>A , LRG_887t1:c.-86C>A | NP_055440.1:n.-86C>A | |
XM_005245483.2:c.-86C>A | XP_005245540.1:n.-86C>A | |
XM_006711529.2:c.-86C>A | XP_006711592.1:n.-86C>A | |
XM_005245483.3:c.-86C>A | XP_005245540.1:n.-86C>A | |
XM_017002298.1:c.-86C>A | XP_016857787.1:n.-86C>A | |
XM_017002299.1:c.-86C>A | XP_016857788.1:n.-86C>A |