HGVS | Genome Assembly |
---|---|
NC_000017.11:g.7454438T>A , CM000679.2:g.7454438T>A | GRCh38 |
NC_000017.10:g.7357757T>A , CM000679.1:g.7357757T>A | GRCh37 |
NC_000017.9:g.7298481T>A | NCBI36 |
NG_008026.1:g.14352T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000306071.7:c.962T>A MANE Select | ENSP00000304290.2:p.Phe321Tyr | |
ENST00000306071.6:c.962T>A | ENSP00000304290.2:p.Phe321Tyr | |
ENST00000536404.6:c.746T>A | ENSP00000439209.2:p.Phe249Tyr | |
ENST00000570557.5:c.625T>A | ||
ENST00000573209.1:n.1906T>A | ||
ENST00000576360.1:c.605-6T>A | ENSP00000459092.1:n.605-6T>A | |
NM_000747.2:c.962T>A | NP_000738.2:p.Phe321Tyr | |
NM_000747.3:c.962T>A MANE Select | NP_000738.2:p.Phe321Tyr |