HGVS | Genome Assembly |
---|---|
NC_000005.10:g.159315948del , CM000667.2:g.159315948del | GRCh38 |
NC_000005.9:g.158742956del , CM000667.1:g.158742956del | GRCh37 |
NC_000005.8:g.158675534del | NCBI36 |
NG_009618.1:g.19526del , LRG_71:g.19526del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000696750.1:c.*153del | ENSP00000512849.1:n.*153del | |
ENST00000696751.1:c.*635del | ENSP00000512850.1:n.*635del | |
ENST00000231228.3:c.*153del MANE Select | ENSP00000231228.2:n.*153del | |
ENST00000231228.2:c.*153del | ENSP00000231228.2:n.*153del | |
NM_002187.2:c.*153del , LRG_71t1:c.*153del | NP_002178.2:n.*153del | |
NM_002187.3:c.*153del MANE Select | NP_002178.2:n.*153del |