HGVS | Genome Assembly |
---|---|
NC_000006.12:g.24306022_24306023del , CM000668.2:g.24306022_24306023del | GRCh38 |
NC_000006.11:g.24306250_24306251del , CM000668.1:g.24306250_24306251del | GRCh37 |
NC_000006.10:g.24414229_24414230del | NCBI36 |
NG_012829.1:g.57032_57033del | |
NG_012829.2:g.82272_82273del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000378454.8:c.349-3977_349-3976del MANE Select | ENSP00000367715.3:n.349-3977_349-3976del | |
ENST00000378454.7:c.349-3977_349-3976del | ENSP00000367715.3:n.349-3977_349-3976del | |
NM_001195610.1:c.349-3977_349-3976del | NP_001182539.1:n.349-3977_349-3976del | |
NM_016356.4:c.349-3977_349-3976del | NP_057440.2:n.349-3977_349-3976del | |
NM_016356.5:c.349-3977_349-3976del MANE Select | NP_057440.2:n.349-3977_349-3976del | |
NM_001195610.2:c.349-3977_349-3976del | NP_001182539.1:n.349-3977_349-3976del |