HGVS | Genome Assembly |
---|---|
NC_000009.12:g.38396908_38396909delinsGC , CM000671.2:g.38396908_38396909delinsGC | GRCh38 |
NC_000009.11:g.38396905_38396906delinsGC , CM000671.1:g.38396905_38396906delinsGC | GRCh37 |
NC_000009.10:g.38386905_38386906delinsGC | NCBI36 |
NG_012253.1:g.9204_9205delinsGC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000377698.4:c.1160_1161delinsGC MANE Select | ENSP00000366927.3:p.Gly387= | |
ENST00000377698.3:c.1160_1161delinsGC | ENSP00000366927.3:p.Gly387= | |
NM_000692.4:c.1160_1161delinsGC | NP_000683.3:p.Gly387= | |
XM_011517802.1:c.1160_1161delinsGC | XP_011516104.1:p.Gly387= | |
XM_011517802.2:c.1160_1161delinsGC | XP_011516104.1:p.Gly387= | |
NM_000692.5:c.1160_1161delinsGC MANE Select | NP_000683.3:p.Gly387= |