HGVS | Genome Assembly |
---|---|
NC_000017.11:g.80099853T= , CM000679.2:g.80099853T= | GRCh38 |
NC_000017.10:g.78073652T= , CM000679.1:g.78073652T= | GRCh37 |
NC_000017.9:g.75688247T= | NCBI36 |
NG_009822.1:g.3298T= , LRG_673:g.3298T= | |
NG_029761.1:g.68222T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000397545.9:c.*78T= MANE Select | ENSP00000380679.4:n.*78T= | |
ENST00000397545.8:c.*78T= | ENSP00000380679.4:n.*78T= | |
ENST00000574799.5:n.3044T= | ||
NM_017950.3:c.*78T= | NP_060420.2:n.*78T= | |
XM_011524963.1:c.*78T= | XP_011523265.1:n.*78T= | |
XM_011524964.1:c.*78T= | XP_011523266.1:n.*78T= | |
XM_011524963.3:c.*78T= | XP_011523265.1:n.*78T= | |
XM_011524964.3:c.*78T= | XP_011523266.1:n.*78T= | |
XM_024450821.1:c.*78T= | XP_024306589.1:n.*78T= | |
XR_934495.2:n.3625T= | ||
NM_017950.4:c.*78T= MANE Select | NP_060420.2:n.*78T= |