HGVS | Genome Assembly |
---|---|
NC_000020.11:g.10412939_10412940delinsGC , CM000682.2:g.10412939_10412940delinsGC | GRCh38 |
NC_000020.10:g.10393587_10393588delinsGC , CM000682.1:g.10393587_10393588delinsGC | GRCh37 |
NC_000020.9:g.10341587_10341588delinsGC | NCBI36 |
NG_009109.1:g.26279_26280delinsGC | |
NG_009109.2:g.26279_26280delinsGC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000651692.1:c.575_576delinsGC | ENSP00000498849.1:p.Gly192= | |
ENST00000652676.1:n.459-240_459-239delinsGC | ||
ENST00000347364.7:c.575_576delinsGC MANE Select | ENSP00000246062.4:p.Gly192= | |
ENST00000399054.6:c.575_576delinsGC | ENSP00000382008.2:p.Gly192= | |
NM_018848.3:c.575_576delinsGC | NP_061336.1:p.Gly192= | |
NM_170784.2:c.575_576delinsGC | NP_740754.1:p.Gly192= | |
NR_072977.1:n.364-4137_364-4136delinsGC | ||
NR_072977.2:n.347-4137_347-4136delinsGC | ||
NM_170784.3:c.575_576delinsGC MANE Select | NP_740754.1:p.Gly192= |