HGVS | Genome Assembly |
---|---|
NC_000009.12:g.38396909C= , CM000671.2:g.38396909C= | GRCh38 |
NC_000009.11:g.38396906C= , CM000671.1:g.38396906C= | GRCh37 |
NC_000009.10:g.38386906C= | NCBI36 |
NG_012253.1:g.9205C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000377698.4:c.1161C= MANE Select | ENSP00000366927.3:p.Gly387= | |
ENST00000377698.3:c.1161C= | ENSP00000366927.3:p.Gly387= | |
NM_000692.4:c.1161C= | NP_000683.3:p.Gly387= | |
XM_011517802.1:c.1161C= | XP_011516104.1:p.Gly387= | |
XM_011517802.2:c.1161C= | XP_011516104.1:p.Gly387= | |
NM_000692.5:c.1161C= MANE Select | NP_000683.3:p.Gly387= |