HGVS | Genome Assembly |
---|---|
NC_000009.12:g.38396571_38396572insC , CM000671.2:g.38396571_38396572insC | GRCh38 |
NC_000009.11:g.38396568_38396569insC , CM000671.1:g.38396568_38396569insC | GRCh37 |
NC_000009.10:g.38386568_38386569insC | NCBI36 |
NG_012253.1:g.8867_8868insC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000377698.4:c.823_824insC MANE Select | ENSP00000366927.3:p.Gly275AlafsTer15 | |
ENST00000377698.3:c.823_824insC | ENSP00000366927.3:p.Gly275AlafsTer15 | |
NM_000692.4:c.823_824insC | NP_000683.3:p.Gly275AlafsTer15 | |
XM_011517802.1:c.823_824insC | XP_011516104.1:p.Gly275AlafsTer15 | |
XM_011517802.2:c.823_824insC | XP_011516104.1:p.Gly275AlafsTer15 | |
NM_000692.5:c.823_824insC MANE Select | NP_000683.3:p.Gly275AlafsTer15 |