HGVS | Genome Assembly |
---|---|
NC_000022.11:g.50625034T>A , CM000684.2:g.50625034T>A | GRCh38 |
NC_000022.10:g.51063462T>A , CM000684.1:g.51063462T>A | GRCh37 |
NC_000022.9:g.49410328T>A | NCBI36 |
NG_009260.2:g.8146A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000216124.10:c.*111A>T MANE Select | ENSP00000216124.5:n.*111A>T | |
ENST00000216124.9:c.*111A>T | ENSP00000216124.5:n.*111A>T | |
ENST00000356098.9:c.*111A>T | ENSP00000348406.5:n.*111A>T | |
ENST00000395619.3:c.*111A>T | ENSP00000378981.3:n.*111A>T | |
ENST00000395621.7:c.*111A>T | ENSP00000378983.3:n.*111A>T | |
ENST00000453344.6:c.*111A>T | ENSP00000412542.2:n.*111A>T | |
ENST00000608497.1:c.180+329A>T | ||
NM_000487.5:c.*111A>T | NP_000478.3:n.*111A>T | |
NM_001085425.2:c.*111A>T | NP_001078894.2:n.*111A>T | |
NM_001085426.2:c.*111A>T | NP_001078895.2:n.*111A>T | |
NM_001085427.2:c.*111A>T | NP_001078896.2:n.*111A>T | |
NM_001085428.2:c.*111A>T | NP_001078897.1:n.*111A>T | |
XM_011530690.1:c.*111A>T | XP_011528992.1:n.*111A>T | |
XM_011530691.1:c.*374A>T | XP_011528993.1:n.*374A>T | |
NM_001362782.1:c.*111A>T | NP_001349711.1:n.*111A>T | |
XM_011530691.3:c.*374A>T | XP_011528993.1:n.*374A>T | |
XM_017028800.1:c.*111A>T | XP_016884289.1:n.*111A>T | |
XM_024452241.1:c.*374A>T | XP_024308009.1:n.*374A>T | |
NM_000487.6:c.*111A>T MANE Select | NP_000478.3:n.*111A>T | |
NM_001085425.3:c.*111A>T | NP_001078894.2:n.*111A>T | |
NM_001085426.3:c.*111A>T | NP_001078895.2:n.*111A>T | |
NM_001085427.3:c.*111A>T | NP_001078896.2:n.*111A>T | |
NM_001085428.3:c.*111A>T | NP_001078897.1:n.*111A>T | |
NM_001362782.2:c.*111A>T | NP_001349711.1:n.*111A>T |