HGVS | Genome Assembly |
---|---|
NC_000009.12:g.128945885A= , CM000671.2:g.128945885A= | GRCh38 |
NC_000009.11:g.131708164A= , CM000671.1:g.131708164A= | GRCh37 |
NC_000009.10:g.130747985A= | NCBI36 |
NG_017009.1:g.6849T= , LRG_744:g.6849T= | |
NG_033111.1:g.3193A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000372586.4:c.1419T= MANE Select | ENSP00000361667.3:p.Phe473= | |
ENST00000372586.3:c.1419T= | ENSP00000361667.3:p.Phe473= | |
ENST00000482796.1:c.39-3304A= | ENSP00000417556.2:n.39-3304A= | |
NM_014908.3:c.1419T= , LRG_744t1:c.1419T= | NP_055723.1:p.Phe473= | |
NM_014908.4:c.1419T= MANE Select | NP_055723.1:p.Phe473= |