HGVS | Genome Assembly |
---|---|
NC_000002.12:g.218882242del , CM000664.2:g.218882242del | GRCh38 |
NC_000002.11:g.219746964del , CM000664.1:g.219746964del | GRCh37 |
NC_000002.10:g.219455208del | NCBI36 |
NG_012179.1:g.6710del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000258411.8:c.195del MANE Select | ENSP00000258411.3:p.Gly66AlafsTer2 | |
ENST00000258411.7:c.195del | ENSP00000258411.3:p.Gly66AlafsTer2 | |
ENST00000458582.1:c.82del | ||
NM_025216.2:c.195del | NP_079492.2:p.Gly66AlafsTer2 | |
XM_011511928.1:c.144del | XP_011510230.1:p.Gly49AlafsTer2 | |
XM_011511929.1:c.99del | XP_011510231.1:p.Gly34AlafsTer2 | |
XM_011511930.1:c.195del | XP_011510232.1:p.Gly66AlafsTer2 | |
XM_011511929.2:c.99del | XP_011510231.1:p.Gly34AlafsTer2 | |
NM_025216.3:c.195del MANE Select | NP_079492.2:p.Gly66AlafsTer2 |