HGVS | Genome Assembly |
---|---|
NC_000001.11:g.209786349A= , CM000663.2:g.209786349A= | GRCh38 |
NC_000001.10:g.209959694A= , CM000663.1:g.209959694A= | GRCh37 |
NC_000001.9:g.208026317A= | NCBI36 |
NG_007081.2:g.24786T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000696133.1:c.1400+2075T= | ENSP00000512426.1:n.1400+2075T= | |
ENST00000696134.1:c.*2902T= | ENSP00000512427.1:n.*2902T= | |
ENST00000367021.8:c.*2071T= MANE Select | ENSP00000355988.3:n.*2071T= | |
ENST00000367021.7:c.*2071T= | ENSP00000355988.3:n.*2071T= | |
ENST00000542854.5:c.*2071T= | ENSP00000440532.1:n.*2071T= | |
NM_001206696.1:c.*2071T= | NP_001193625.1:n.*2071T= | |
NM_006147.3:c.*2071T= | NP_006138.1:n.*2071T= | |
NM_006147.4:c.*2071T= MANE Select | NP_006138.1:n.*2071T= | |
NM_001206696.2:c.*2071T= | NP_001193625.1:n.*2071T= |