HGVS | Genome Assembly |
---|---|
NC_000007.14:g.128247215_128247225del , CM000669.2:g.128247215_128247225del | GRCh38 |
NC_000007.13:g.127887268_127887278del , CM000669.1:g.127887268_127887278del | GRCh37 |
NC_000007.12:g.127674504_127674514del | NCBI36 |
NG_007450.1:g.10938_10948del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000308868.5:c.-28-4776_-28-4766del MANE Select | ENSP00000312652.4:n.-28-4776_-28-4766del | |
ENST00000308868.4:c.-28-4776_-28-4766del | ENSP00000312652.4:n.-28-4776_-28-4766del | |
NM_000230.2:c.-28-4776_-28-4766del | NP_000221.1:n.-28-4776_-28-4766del | |
XM_005250340.3:c.-28-4776_-28-4766del | XP_005250397.1:n.-28-4776_-28-4766del | |
XM_005250340.5:c.-28-4776_-28-4766del | XP_005250397.1:n.-28-4776_-28-4766del | |
NM_000230.3:c.-28-4776_-28-4766del MANE Select | NP_000221.1:n.-28-4776_-28-4766del |