HGVS | Genome Assembly |
---|---|
NC_000006.12:g.1609958_1609960delinsGGC , CM000668.2:g.1609958_1609960delinsGGC | GRCh38 |
NC_000006.11:g.1610193_1610195delinsGGC , CM000668.1:g.1610193_1610195delinsGGC | GRCh37 |
NC_000006.10:g.1555192_1555194delinsGGC | NCBI36 |
NG_009368.1:g.4513_4515delinsGGC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000645831.2:c.-488_-486delinsGGC MANE Select | ENSP00000493906.1:n.-488_-486delinsGGC | |
NM_001453.3:c.-488_-486delinsGGC MANE Select | NP_001444.2:n.-488_-486delinsGGC |