HGVS | Genome Assembly |
---|---|
NC_000023.11:g.53378192C= , CM000685.2:g.53378192C= | GRCh38 |
NC_000023.10:g.53405113C= , CM000685.1:g.53405113C= | GRCh37 |
NC_000023.9:g.53421838C= | NCBI36 |
NG_006988.2:g.49479G= , LRG_773:g.49479G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000322213.9:c.*1911G= MANE Select | ENSP00000323421.3:n.*1911G= | |
ENST00000675504.1:c.*1911G= | ENSP00000502524.1:n.*1911G= | |
ENST00000322213.8:c.*1911G= | ENSP00000323421.3:n.*1911G= | |
ENST00000375340.10:c.*1911G= | ENSP00000364489.7:n.*1911G= | |
NM_001281463.1:c.*1911G= , LRG_773t1:c.*1911G= | NP_001268392.1:n.*1911G= | |
NM_006306.3:c.*1911G= , LRG_773t2:c.*1911G= | NP_006297.2:n.*1911G= | |
NM_006306.4:c.*1911G= MANE Select | NP_006297.2:n.*1911G= |