HGVS | Genome Assembly |
---|---|
NC_000003.12:g.37476003_37476006delinsATGT , CM000665.2:g.37476003_37476006delinsATGT | GRCh38 |
NC_000003.11:g.37517494_37517497delinsATGT , CM000665.1:g.37517494_37517497delinsATGT | GRCh37 |
NC_000003.10:g.37492498_37492501delinsATGT | NCBI36 |
NG_016166.1:g.28682_28685delinsATGT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000264741.10:c.420+2543_420+2546delinsATGT MANE Select | ENSP00000264741.5:n.420+2543_420+2546deli... | |
ENST00000264741.9:c.420+2543_420+2546delinsATGT | ENSP00000264741.5:n.420+2543_420+2546deli... | |
ENST00000422441.5:c.420+2543_420+2546delinsATGT | ENSP00000397258.1:n.420+2543_420+2546deli... | |
NM_002207.2:c.420+2543_420+2546delinsATGT | NP_002198.2:n.420+2543_420+2546delinsATGT... | |
NM_002207.3:c.420+2543_420+2546delinsATGT MANE Select | NP_002198.2:n.420+2543_420+2546delinsATGT... |