HGVS | Genome Assembly |
---|---|
NC_000015.10:g.73322774_73322775delinsGC , CM000677.2:g.73322774_73322775delinsGC | GRCh38 |
NC_000015.9:g.73615115_73615116delinsGC , CM000677.1:g.73615115_73615116delinsGC | GRCh37 |
NC_000015.8:g.71402168_71402169delinsGC | NCBI36 |
NG_009063.1:g.51490_51491delinsGC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261917.4:c.3318_3319delinsGC MANE Select | ENSP00000261917.3:p.Pro1106= | |
ENST00000261917.3:c.3318_3319delinsGC | ENSP00000261917.3:p.Pro1106= | |
NM_005477.2:c.3318_3319delinsGC | NP_005468.1:p.Pro1106= | |
XM_011521148.1:c.2100_2101delinsGC | XP_011519450.1:p.Pro700= | |
XM_011521148.2:c.2100_2101delinsGC | XP_011519450.1:p.Pro700= | |
NM_005477.3:c.3318_3319delinsGC MANE Select | NP_005468.1:p.Pro1106= |