HGVS | Genome Assembly |
---|---|
NC_000011.10:g.5253200T= , CM000673.2:g.5253200T= | GRCh38 |
NC_000011.9:g.5274430T= , CM000673.1:g.5274430T= | GRCh37 |
NC_000011.8:g.5231006T= | NCBI36 |
NG_000007.3:g.44416A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000336906.6:c.*77A= MANE Select | ENSP00000338082.4:n.*77A= | |
ENST00000380252.6:c.*77A= | ENSP00000369602.2:n.*77A= | |
ENST00000642908.1:c.315+1092A= | ENSP00000495346.1:n.315+1092A= | |
ENST00000647543.1:c.378+143A= | ENSP00000496470.1:n.378+143A= | |
ENST00000380252.5:c.*77A= | ENSP00000369602.1:n.*77A= | |
ENST00000380259.6:c.*77A= | ENSP00000369609.2:n.*77A= | |
ENST00000620888.4:c.315+1092A= | ENSP00000479637.1:n.315+1092A= | |
NM_000184.2:c.*77A= | NP_000175.1:n.*77A= | |
NM_000184.3:c.*77A= MANE Select | NP_000175.1:n.*77A= |