HGVS | Genome Assembly |
---|---|
NC_000006.12:g.10897437T>G , CM000668.2:g.10897437T>G | GRCh38 |
NC_000006.11:g.10897670T>G , CM000668.1:g.10897670T>G | GRCh37 |
NC_000006.10:g.11005656T>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000283141.11:c.337-574T>G MANE Select | ENSP00000283141.6:n.337-574T>G | |
ENST00000283141.10:c.337-574T>G | ENSP00000283141.6:n.337-574T>G | |
ENST00000341041.8:c.337-574T>G | ENSP00000340320.4:n.337-574T>G | |
ENST00000480294.1:c.*299-574T>G | ENSP00000417929.1:n.*299-574T>G | |
ENST00000543878.5:c.334-574T>G | ENSP00000440676.2:n.334-574T>G | |
NM_001040274.2:c.337-574T>G | NP_001035364.2:n.337-574T>G | |
NM_001040274.3:c.337-574T>G MANE Select | NP_001035364.2:n.337-574T>G |