HGVS | Genome Assembly |
---|---|
NC_000012.12:g.121626925T= , CM000674.2:g.121626925T= | GRCh38 |
NC_000012.10:g.120549214T= | NCBI36 |
NG_007500.1:g.5351T= , LRG_93:g.5351T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000698901.1:n.417T= | ||
ENST00000617316.2:c.178T= | ENSP00000482568.2:p.Tyr60= | |
ENST00000646827.1:n.376T= | ||
ENST00000611718.1:c.-12T= | ENSP00000477953.1:n.-12T= | |
ENST00000616379.1:c.178T= | ENSP00000480616.1:p.Tyr60= | |
ENST00000617316.1:c.-12T= | ENSP00000482568.1:n.-12T= | |
NM_032790.3:c.178T= , LRG_93t1:c.178T= | NP_116179.2:p.Tyr60= |