HGVS | Genome Assembly |
---|---|
NC_000002.12:g.43887142_43887143del , CM000664.2:g.43887142_43887143del | GRCh38 |
NC_000002.11:g.44114281_44114282del , CM000664.1:g.44114281_44114282del | GRCh37 |
NC_000002.10:g.43967785_43967786del | NCBI36 |
NG_008247.1:g.113865_113866del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000682612.1:c.2411_2412del | ||
ENST00000684454.1:n.9508_9509del | ||
ENST00000260665.12:c.*1459_*1460del MANE Select | ENSP00000260665.7:n.*1459_*1460del | |
ENST00000260665.11:c.*1459_*1460del | ENSP00000260665.7:n.*1459_*1460del | |
NM_133259.3:c.*1459_*1460del | NP_573566.2:n.*1459_*1460del | |
XR_002958896.1:n.5826_5827del | ||
NM_133259.4:c.*1459_*1460del MANE Select | NP_573566.2:n.*1459_*1460del |