HGVS | Genome Assembly |
---|---|
NC_000006.12:g.36685808A= , CM000668.2:g.36685808A= | GRCh38 |
NC_000006.11:g.36653585A= , CM000668.1:g.36653585A= | GRCh37 |
NC_000006.10:g.36761563A= | NCBI36 |
NG_009364.1:g.12127A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000244741.10:c.*8A= MANE Select | ENSP00000244741.6:n.*8A= | |
ENST00000244741.9:c.*8A= | ENSP00000244741.5:n.*8A= | |
ENST00000373711.3:c.*8A= | ENSP00000362815.1:n.*8A= | |
ENST00000405375.5:c.*8A= | ENSP00000384849.1:n.*8A= | |
ENST00000448526.6:c.*8A= | ENSP00000409259.3:n.*8A= | |
ENST00000615513.4:c.*8A= | ENSP00000482768.1:n.*8A= | |
NM_000389.4:c.*8A= | NP_000380.1:n.*8A= | |
NM_001220777.1:c.*8A= | NP_001207706.1:n.*8A= | |
NM_001220778.1:c.*8A= | NP_001207707.1:n.*8A= | |
NM_001291549.1:c.*8A= | NP_001278478.1:n.*8A= | |
NM_078467.2:c.*8A= | NP_510867.1:n.*8A= | |
NM_000389.5:c.*8A= MANE Select | NP_000380.1:n.*8A= | |
NM_001220777.2:c.*8A= | NP_001207706.1:n.*8A= | |
NM_001220778.2:c.*8A= | NP_001207707.1:n.*8A= | |
NM_001291549.3:c.*8A= | NP_001278478.1:n.*8A= | |
NM_001374509.1:c.*8A= | NP_001361438.1:n.*8A= | |
NM_001374510.1:c.*8A= | NP_001361439.1:n.*8A= | |
NM_001374511.1:c.*8A= | NP_001361440.1:n.*8A= | |
NM_001374512.1:c.*298A= | NP_001361441.1:n.*298A= | |
NM_001374513.1:c.*8A= | NP_001361442.1:n.*8A= | |
NM_078467.3:c.*8A= | NP_510867.1:n.*8A= |