HGVS | Genome Assembly |
---|---|
NC_000004.12:g.186191795del , CM000666.2:g.186191795del | GRCh38 |
NC_000004.11:g.187112949del , CM000666.1:g.187112949del | GRCh37 |
NC_000004.10:g.187349943del | NCBI36 |
NG_007965.1:g.5276del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000378802.5:c.-29del MANE Select | ENSP00000368079.4:n.-29del | |
ENST00000378802.4:c.-29del | ENSP00000368079.4:n.-29del | |
NM_207352.3:c.-29del | NP_997235.3:n.-29del | |
XM_005262935.2:c.-29del | XP_005262992.1:n.-29del | |
XM_005262935.4:c.-29del | XP_005262992.1:n.-29del | |
XM_017008037.1:c.-339del | XP_016863526.1:n.-339del | |
NM_207352.4:c.-29del MANE Select | NP_997235.3:n.-29del |