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