HGVS | Genome Assembly |
---|---|
NC_000018.10:g.60371522A= , CM000680.2:g.60371522A= | GRCh38 |
NC_000018.9:g.58038755A= , CM000680.1:g.58038755A= | GRCh37 |
NC_000018.8:g.56189735A= | NCBI36 |
NG_016441.1:g.6247T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000299766.5:c.828T= MANE Select | ENSP00000299766.3:p.Tyr276= | |
ENST00000299766.4:c.828T= | ENSP00000299766.3:p.Tyr276= | |
NM_005912.2:c.828T= | NP_005903.2:p.Tyr276= | |
NM_005912.3:c.828T= MANE Select | NP_005903.2:p.Tyr276= |