HGVS | Genome Assembly |
---|---|
NC_000006.12:g.24206895_24206896del , CM000668.2:g.24206895_24206896del | GRCh38 |
NC_000006.11:g.24207123_24207124del , CM000668.1:g.24207123_24207124del | GRCh37 |
NC_000006.10:g.24315102_24315103del | NCBI36 |
NG_012829.1:g.156160_156161del | |
NG_012829.2:g.181400_181401del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000378454.8:c.923-1791_923-1790del MANE Select | ENSP00000367715.3:n.923-1791_923-1790del | |
ENST00000378454.7:c.923-1791_923-1790del | ENSP00000367715.3:n.923-1791_923-1790del | |
NM_001195610.1:c.923-1791_923-1790del | NP_001182539.1:n.923-1791_923-1790del | |
NM_016356.4:c.923-1791_923-1790del | NP_057440.2:n.923-1791_923-1790del | |
NM_016356.5:c.923-1791_923-1790del MANE Select | NP_057440.2:n.923-1791_923-1790del | |
NM_001195610.2:c.923-1791_923-1790del | NP_001182539.1:n.923-1791_923-1790del |