HGVS | Genome Assembly |
---|---|
NC_000002.12:g.84431667del , CM000664.2:g.84431667del | GRCh38 |
NC_000002.11:g.84658791del , CM000664.1:g.84658791del | GRCh37 |
NC_000002.10:g.84512302del | NCBI36 |
NG_016755.1:g.32800del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000393868.7:c.674-4del MANE Select | ENSP00000377446.2:n.674-4del | |
ENST00000651342.1:c.*114-4del | ENSP00000498471.1:n.*114-4del | |
ENST00000393868.6:c.674-4del | ENSP00000377446.2:n.674-4del | |
ENST00000487809.1:n.421-4del | ||
ENST00000491123.5:n.520-4del | ||
NM_003849.3:c.674-4del | NP_003840.2:n.674-4del | |
NM_003849.4:c.674-4del MANE Select | NP_003840.2:n.674-4del |