HGVS | Genome Assembly |
---|---|
NC_000010.11:g.122506823G>T , CM000672.2:g.122506823G>T | GRCh38 |
NC_000010.10:g.124266339G>T , CM000672.1:g.124266339G>T | GRCh37 |
NC_000010.9:g.124256329G>T | NCBI36 |
NG_011554.1:g.50299G>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000368984.8:c.910G>T MANE Select | ENSP00000357980.3:p.Gly304Cys | |
ENST00000648167.1:c.592G>T | ENSP00000498033.1:p.Gly198Cys | |
ENST00000368984.7:c.910G>T | ENSP00000357980.3:p.Gly304Cys | |
ENST00000420892.1:c.133G>T | ENSP00000412676.1:p.Gly45Cys | |
NM_002775.4:c.910G>T | NP_002766.1:p.Gly304Cys | |
NM_002775.5:c.910G>T MANE Select | NP_002766.1:p.Gly304Cys |