HGVS | Genome Assembly |
---|---|
NC_000010.11:g.122506822C= , CM000672.2:g.122506822C= | GRCh38 |
NC_000010.10:g.124266338C= , CM000672.1:g.124266338C= | GRCh37 |
NC_000010.9:g.124256328C= | NCBI36 |
NG_011554.1:g.50298C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000368984.8:c.909C= MANE Select | ENSP00000357980.3:p.Gly303= | |
ENST00000648167.1:c.591C= | ENSP00000498033.1:p.Gly197= | |
ENST00000368984.7:c.909C= | ENSP00000357980.3:p.Gly303= | |
ENST00000420892.1:c.132C= | ENSP00000412676.1:p.Gly44= | |
NM_002775.4:c.909C= | NP_002766.1:p.Gly303= | |
NM_002775.5:c.909C= MANE Select | NP_002766.1:p.Gly303= |