HGVS | Genome Assembly |
---|---|
NC_000001.11:g.1014139G= , CM000663.2:g.1014139G= | GRCh38 |
NC_000001.10:g.949519G= , CM000663.1:g.949519G= | GRCh37 |
NC_000001.9:g.939382G= | NCBI36 |
NG_033033.1:g.5673G= | |
NG_033033.2:g.18002G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000624697.4:c.135G= | ENSP00000485643.1:p.Ala45= | |
ENST00000649529.1:c.159G= MANE Select | ENSP00000496832.1:p.Ala53= | |
ENST00000379389.4:c.159G= | ENSP00000368699.4:p.Ala53= | |
ENST00000624652.1:c.135G= | ENSP00000485313.1:p.Ala45= | |
ENST00000624697.3:c.135G= | ENSP00000485643.1:p.Ala45= | |
NM_005101.3:c.159G= | NP_005092.1:p.Ala53= | |
NM_005101.4:c.159G= MANE Select | NP_005092.1:p.Ala53= |