HGVS | Genome Assembly |
---|---|
NC_000010.11:g.122506768G>A , CM000672.2:g.122506768G>A | GRCh38 |
NC_000010.10:g.124266284G>A , CM000672.1:g.124266284G>A | GRCh37 |
NC_000010.9:g.124256274G>A | NCBI36 |
NG_011554.1:g.50244G>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000368984.8:c.855G>A MANE Select | ENSP00000357980.3:p.Pro285= | |
ENST00000648167.1:c.537G>A | ENSP00000498033.1:p.Pro179= | |
ENST00000368984.7:c.855G>A | ENSP00000357980.3:p.Pro285= | |
ENST00000420892.1:c.78G>A | ENSP00000412676.1:p.Pro26= | |
NM_002775.4:c.855G>A | NP_002766.1:p.Pro285= | |
NM_002775.5:c.855G>A MANE Select | NP_002766.1:p.Pro285= |