HGVS | Genome Assembly |
---|---|
NC_000018.10:g.60371455G>A , CM000680.2:g.60371455G>A | GRCh38 |
NC_000018.9:g.58038688G>A , CM000680.1:g.58038688G>A | GRCh37 |
NC_000018.8:g.56189668G>A | NCBI36 |
NG_016441.1:g.6314C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000299766.5:c.895C>T MANE Select | ENSP00000299766.3:p.Pro299Ser | |
ENST00000299766.4:c.895C>T | ENSP00000299766.3:p.Pro299Ser | |
NM_005912.2:c.895C>T | NP_005903.2:p.Pro299Ser | |
NM_005912.3:c.895C>T MANE Select | NP_005903.2:p.Pro299Ser |