HGVS | Genome Assembly |
---|---|
NC_000018.10:g.60371536G>T , CM000680.2:g.60371536G>T | GRCh38 |
NC_000018.9:g.58038769G>T , CM000680.1:g.58038769G>T | GRCh37 |
NC_000018.8:g.56189749G>T | NCBI36 |
NG_016441.1:g.6233C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000299766.5:c.814C>A MANE Select | ENSP00000299766.3:p.Pro272Thr | |
ENST00000299766.4:c.814C>A | ENSP00000299766.3:p.Pro272Thr | |
NM_005912.2:c.814C>A | NP_005903.2:p.Pro272Thr | |
NM_005912.3:c.814C>A MANE Select | NP_005903.2:p.Pro272Thr |