HGVS | Genome Assembly |
---|---|
NC_000006.12:g.24290829_24290832del , CM000668.2:g.24290829_24290832del | GRCh38 |
NC_000006.11:g.24291057_24291060del , CM000668.1:g.24291057_24291060del | GRCh37 |
NC_000006.10:g.24399036_24399039del | NCBI36 |
NG_012829.1:g.72226_72229del | |
NG_012829.2:g.97466_97469del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000378454.8:c.704+105_704+108del MANE Select | ENSP00000367715.3:n.704+105_704+108del | |
ENST00000378454.7:c.704+105_704+108del | ENSP00000367715.3:n.704+105_704+108del | |
NM_001195610.1:c.704+105_704+108del | NP_001182539.1:n.704+105_704+108del | |
NM_016356.4:c.704+105_704+108del | NP_057440.2:n.704+105_704+108del | |
NM_016356.5:c.704+105_704+108del MANE Select | NP_057440.2:n.704+105_704+108del | |
NM_001195610.2:c.704+105_704+108del | NP_001182539.1:n.704+105_704+108del |