HGVS | Genome Assembly |
---|---|
NC_000004.12:g.24800318del , CM000666.2:g.24800318del | GRCh38 |
NC_000004.11:g.24801940del , CM000666.1:g.24801940del | GRCh37 |
NC_000004.10:g.24411038del | NCBI36 |
NG_012213.1:g.9856del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382120.4:c.*74del MANE Select | ENSP00000371554.3:n.*74del | |
ENST00000382120.3:c.*74del | ENSP00000371554.3:n.*74del | |
NM_003102.2:c.*74del | NP_003093.2:n.*74del | |
XR_427488.1:n.987del | ||
NM_003102.3:c.*74del | NP_003093.2:n.*74del | |
NM_003102.4:c.*74del MANE Select | NP_003093.2:n.*74del |