HGVS | Genome Assembly |
---|---|
NC_000005.10:g.1414393_1414425del , CM000667.2:g.1414393_1414425del | GRCh38 |
NC_000005.9:g.1414508_1414540del , CM000667.1:g.1414508_1414540del | GRCh37 |
NC_000005.8:g.1467508_1467540del | NCBI36 |
NG_015885.1:g.36004_36036del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000270349.12:c.1156+266_1156+298del MANE Select | ENSP00000270349.9:n.1156+266_1156+298del | |
ENST00000270349.11:c.1156+266_1156+298del | ENSP00000270349.9:n.1156+266_1156+298del | |
NM_001044.4:c.1156+266_1156+298del | NP_001035.1:n.1156+266_1156+298del | |
NM_001044.5:c.1156+266_1156+298del MANE Select | NP_001035.1:n.1156+266_1156+298del |