HGVS | Genome Assembly |
---|---|
NC_000010.11:g.122461915A= , CM000672.2:g.122461915A= | GRCh38 |
NC_000010.10:g.124221431A= , CM000672.1:g.124221431A= | GRCh37 |
NC_000010.9:g.124211421A= | NCBI36 |
NG_011554.1:g.5391A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000368984.8:c.263A= MANE Select | ENSP00000357980.3:p.Gln88= | |
ENST00000648167.1:c.154+3206A= | ENSP00000498033.1:n.154+3206A= | |
ENST00000368984.7:c.263A= | ENSP00000357980.3:p.Gln88= | |
NM_002775.4:c.263A= | NP_002766.1:p.Gln88= | |
NM_002775.5:c.263A= MANE Select | NP_002766.1:p.Gln88= |