HGVS | Genome Assembly |
---|---|
NC_000021.9:g.45984270T= , CM000683.2:g.45984270T= | GRCh38 |
NC_000021.8:g.47404184T= , CM000683.1:g.47404184T= | GRCh37 |
NC_000021.7:g.46228612T= | NCBI36 |
NG_008674.1:g.7522T= , LRG_475:g.7522T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361866.8:c.229T= MANE Select | ENSP00000355180.3:p.Tyr77= | |
ENST00000361866.7:c.229T= | ENSP00000355180.3:p.Tyr77= | |
ENST00000612273.1:c.229T= | ENSP00000483630.1:p.Tyr77= | |
NM_001848.2:c.229T= , LRG_475t1:c.229T= | NP_001839.2:p.Tyr77= | |
NM_001848.3:c.229T= MANE Select | NP_001839.2:p.Tyr77= |