HGVS | Genome Assembly |
---|---|
NC_000017.11:g.4631508G>T , CM000679.2:g.4631508G>T | GRCh38 |
NC_000017.10:g.4534803G>T , CM000679.1:g.4534803G>T | GRCh37 |
NC_000017.9:g.4481552G>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000293761.8:c.*92C>A MANE Select | ENSP00000293761.3:n.*92C>A | |
ENST00000570836.6:c.*92C>A | ENSP00000458832.1:n.*92C>A | |
ENST00000293761.7:c.*92C>A | ENSP00000293761.3:n.*92C>A | |
ENST00000570836.5:c.*92C>A | ENSP00000458832.1:n.*92C>A | |
ENST00000574640.1:c.*92C>A | ENSP00000460483.1:n.*92C>A | |
NM_001140.3:c.*92C>A | NP_001131.3:n.*92C>A | |
NM_001140.4:c.*92C>A | NP_001131.3:n.*92C>A | |
NM_001140.5:c.*92C>A MANE Select | NP_001131.3:n.*92C>A |