HGVS | Genome Assembly |
---|---|
NC_000005.10:g.159316008del , CM000667.2:g.159316008del | GRCh38 |
NC_000005.9:g.158743016del , CM000667.1:g.158743016del | GRCh37 |
NC_000005.8:g.158675594del | NCBI36 |
NG_009618.1:g.19466del , LRG_71:g.19466del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000696750.1:c.*93del | ENSP00000512849.1:n.*93del | |
ENST00000696751.1:c.*575del | ENSP00000512850.1:n.*575del | |
ENST00000231228.3:c.*93del MANE Select | ENSP00000231228.2:n.*93del | |
ENST00000231228.2:c.*93del | ENSP00000231228.2:n.*93del | |
NM_002187.2:c.*93del , LRG_71t1:c.*93del | NP_002178.2:n.*93del | |
NM_002187.3:c.*93del MANE Select | NP_002178.2:n.*93del |