HGVS | Genome Assembly |
---|---|
NC_000002.12:g.72891671del , CM000664.2:g.72891671del | GRCh38 |
NC_000002.11:g.73118800del , CM000664.1:g.73118800del | GRCh37 |
NC_000002.10:g.72972308del | NCBI36 |
NG_008234.1:g.9289del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000234454.6:c.*134del MANE Select | ENSP00000234454.5:n.*134del | |
ENST00000234454.5:c.*134del | ENSP00000234454.5:n.*134del | |
ENST00000498749.1:n.865del | ||
NM_003124.4:c.*134del | NP_003115.1:n.*134del | |
NM_003124.5:c.*134del MANE Select | NP_003115.1:n.*134del |