HGVS | Genome Assembly |
---|---|
NC_000021.9:g.45984425C>G , CM000683.2:g.45984425C>G | GRCh38 |
NC_000021.8:g.47404339C>G , CM000683.1:g.47404339C>G | GRCh37 |
NC_000021.7:g.46228767C>G | NCBI36 |
NG_008674.1:g.7677C>G , LRG_475:g.7677C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361866.8:c.384C>G MANE Select | ENSP00000355180.3:p.Tyr128Ter | |
ENST00000361866.7:c.384C>G | ENSP00000355180.3:p.Tyr128Ter | |
ENST00000612273.1:c.384C>G | ENSP00000483630.1:p.Tyr128Ter | |
NM_001848.2:c.384C>G , LRG_475t1:c.384C>G | NP_001839.2:p.Tyr128Ter | |
NM_001848.3:c.384C>G MANE Select | NP_001839.2:p.Tyr128Ter |