HGVS | Genome Assembly |
---|---|
NC_000018.10:g.60371471A>C , CM000680.2:g.60371471A>C | GRCh38 |
NC_000018.9:g.58038704A>C , CM000680.1:g.58038704A>C | GRCh37 |
NC_000018.8:g.56189684A>C | NCBI36 |
NG_016441.1:g.6298T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000299766.5:c.879T>G MANE Select | ENSP00000299766.3:p.Cys293Trp | |
ENST00000299766.4:c.879T>G | ENSP00000299766.3:p.Cys293Trp | |
NM_005912.2:c.879T>G | NP_005903.2:p.Cys293Trp | |
NM_005912.3:c.879T>G MANE Select | NP_005903.2:p.Cys293Trp |