HGVS | Genome Assembly |
---|---|
NC_000011.10:g.639988_640044del , CM000673.2:g.639988_640044del | GRCh38 |
NC_000011.9:g.639988_640044del , CM000673.1:g.639988_640044del | GRCh37 |
NC_000011.8:g.629988_630044del | NCBI36 |
NG_021241.1:g.7684_7740del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000176183.6:c.739_795del MANE Select | ENSP00000176183.5:p.Thr247_Pro265del | |
ENST00000176183.5:c.739_795del | ENSP00000176183.5:p.Thr247_Pro265del | |
NM_000797.3:c.739_795del | NP_000788.2:p.Thr247_Pro265del | |
NM_000797.4:c.739_795del MANE Select | NP_000788.2:p.Thr247_Pro265del |