HGVS | Genome Assembly |
---|---|
NC_000006.12:g.10982279A>G , CM000668.2:g.10982279A>G | GRCh38 |
NC_000006.11:g.10982512A>G , CM000668.1:g.10982512A>G | GRCh37 |
NC_000006.10:g.11090498A>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000354666.4:c.*1502T>C MANE Select | ENSP00000346693.3:n.*1502T>C | |
ENST00000354666.3:c.*1502T>C | ENSP00000346693.3:n.*1502T>C | |
NM_017770.3:c.*1502T>C | NP_060240.3:n.*1502T>C | |
XM_011514716.1:c.*1502T>C | XP_011513018.1:n.*1502T>C | |
XM_011514717.1:c.*1502T>C | XP_011513019.1:n.*1502T>C | |
XM_011514716.3:c.*1502T>C | XP_011513018.1:n.*1502T>C | |
NM_017770.4:c.*1502T>C MANE Select | NP_060240.3:n.*1502T>C |