HGVS | Genome Assembly |
---|---|
NC_000009.12:g.38396416C>A , CM000671.2:g.38396416C>A | GRCh38 |
NC_000009.11:g.38396413C>A , CM000671.1:g.38396413C>A | GRCh37 |
NC_000009.10:g.38386413C>A | NCBI36 |
NG_012253.1:g.8712C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000377698.4:c.668C>A MANE Select | ENSP00000366927.3:p.Ser223Tyr | |
ENST00000377698.3:c.668C>A | ENSP00000366927.3:p.Ser223Tyr | |
NM_000692.4:c.668C>A | NP_000683.3:p.Ser223Tyr | |
XM_011517802.1:c.668C>A | XP_011516104.1:p.Ser223Tyr | |
XM_011517802.2:c.668C>A | XP_011516104.1:p.Ser223Tyr | |
NM_000692.5:c.668C>A MANE Select | NP_000683.3:p.Ser223Tyr |