HGVS | Genome Assembly |
---|---|
NC_000009.12:g.128945610del , CM000671.2:g.128945610del | GRCh38 |
NC_000009.11:g.131707889del , CM000671.1:g.131707889del | GRCh37 |
NC_000009.10:g.130747710del | NCBI36 |
NG_017009.1:g.7126del , LRG_744:g.7126del | |
NG_033111.1:g.2918del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000372586.4:c.*79del MANE Select | ENSP00000361667.3:n.*79del | |
ENST00000372586.3:c.*79del | ENSP00000361667.3:n.*79del | |
ENST00000482796.1:c.39-3579del | ENSP00000417556.2:n.39-3579del | |
NM_014908.3:c.*79del , LRG_744t1:c.*79del | NP_055723.1:n.*79del | |
NM_014908.4:c.*79del MANE Select | NP_055723.1:n.*79del |