HGVS | Genome Assembly |
---|---|
NC_000015.10:g.73367869del , CM000677.2:g.73367869del | GRCh38 |
NC_000015.9:g.73660210del , CM000677.1:g.73660210del | GRCh37 |
NC_000015.8:g.71447263del | NCBI36 |
NG_009063.1:g.6398del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261917.4:c.404del MANE Select | ENSP00000261917.3:p.Gly135AlafsTer? | |
ENST00000261917.3:c.404del | ENSP00000261917.3:p.Gly135AlafsTer? | |
NM_005477.2:c.404del | NP_005468.1:p.Gly135AlafsTer? | |
NM_005477.3:c.404del MANE Select | NP_005468.1:p.Gly135AlafsTer? |