HGVS | Genome Assembly |
---|---|
NC_000004.12:g.186191709_186191710delinsGA , CM000666.2:g.186191709_186191710delinsGA | GRCh38 |
NC_000004.11:g.187112863_187112864delinsGA , CM000666.1:g.187112863_187112864delinsGA | GRCh37 |
NC_000004.10:g.187349857_187349858delinsGA | NCBI36 |
NG_007965.1:g.5190_5191delinsGA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000378802.5:c.-115_-114delinsGA MANE Select | ENSP00000368079.4:n.-115_-114delinsGA | |
ENST00000378802.4:c.-115_-114delinsGA | ENSP00000368079.4:n.-115_-114delinsGA | |
NM_207352.3:c.-115_-114delinsGA | NP_997235.3:n.-115_-114delinsGA | |
XM_005262935.2:c.-115_-114delinsGA | XP_005262992.1:n.-115_-114delinsGA | |
XM_017008037.1:c.-425_-424delinsGA | XP_016863526.1:n.-425_-424delinsGA | |
NM_207352.4:c.-115_-114delinsGA MANE Select | NP_997235.3:n.-115_-114delinsGA |