HGVS | Genome Assembly |
---|---|
NC_000005.10:g.159315924del , CM000667.2:g.159315924del | GRCh38 |
NC_000005.9:g.158742932del , CM000667.1:g.158742932del | GRCh37 |
NC_000005.8:g.158675510del | NCBI36 |
NG_009618.1:g.19550del , LRG_71:g.19550del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000696750.1:c.*177del | ENSP00000512849.1:n.*177del | |
ENST00000696751.1:c.*659del | ENSP00000512850.1:n.*659del | |
ENST00000231228.3:c.*177del MANE Select | ENSP00000231228.2:n.*177del | |
ENST00000231228.2:c.*177del | ENSP00000231228.2:n.*177del | |
NM_002187.2:c.*177del , LRG_71t1:c.*177del | NP_002178.2:n.*177del | |
NM_002187.3:c.*177del MANE Select | NP_002178.2:n.*177del |