HGVS | Genome Assembly |
---|---|
NC_000002.12:g.84425641_84425643del , CM000664.2:g.84425641_84425643del | GRCh38 |
NC_000002.11:g.84652765_84652767del , CM000664.1:g.84652765_84652767del | GRCh37 |
NC_000002.10:g.84506276_84506278del | NCBI36 |
NG_016755.1:g.38824_38826del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000393868.7:c.826-36_826-34del MANE Select | ENSP00000377446.2:n.826-36_826-34del | |
ENST00000651342.1:c.*266-36_*266-34del | ENSP00000498471.1:n.*266-36_*266-34del | |
ENST00000393868.6:c.826-36_826-34del | ENSP00000377446.2:n.826-36_826-34del | |
ENST00000484365.1:n.1298_1300del | ||
ENST00000487809.1:n.573-36_573-34del | ||
ENST00000491123.5:n.672-36_672-34del | ||
NM_003849.3:c.826-36_826-34del | NP_003840.2:n.826-36_826-34del | |
NM_003849.4:c.826-36_826-34del MANE Select | NP_003840.2:n.826-36_826-34del |