HGVS | Genome Assembly |
---|---|
NC_000019.10:g.7934043G= , CM000681.2:g.7934043G= | GRCh38 |
NC_000019.9:g.7998928G= , CM000681.1:g.7998928G= | GRCh37 |
NC_000019.8:g.7904928G= | NCBI36 |
NG_051180.1:g.14781C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000270538.8:c.544-40C= MANE Select | ENSP00000270538.2:n.544-40C= | |
ENST00000270538.7:c.544-40C= | ENSP00000270538.2:n.544-40C= | |
ENST00000595831.5:c.531-40C= | ||
ENST00000595876.5:c.*232-40C= | ENSP00000471596.1:n.*232-40C= | |
ENST00000597926.1:c.448-40C= | ENSP00000469389.1:n.448-40C= | |
ENST00000600748.5:n.529-40C= | ||
NM_006351.3:c.544-40C= | NP_006342.2:n.544-40C= | |
NM_006351.4:c.544-40C= MANE Select | NP_006342.2:n.544-40C= |