HGVS | Genome Assembly |
---|---|
NC_000011.10:g.67483151G= , CM000673.2:g.67483151G= | GRCh38 |
NC_000011.9:g.67250622G= , CM000673.1:g.67250622G= | GRCh37 |
NC_000011.8:g.67007198G= | NCBI36 |
NG_008969.1:g.5118G= , LRG_460:g.5118G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000528641.7:c.-8G= | ENSP00000434982.3:n.-8G= | |
ENST00000682324.1:c.-8G= | ENSP00000508017.1:n.-8G= | |
ENST00000682699.1:c.-8G= | ENSP00000507935.1:n.-8G= | |
ENST00000683237.1:c.-8G= | ENSP00000507343.1:n.-8G= | |
ENST00000684006.1:c.-8G= | ENSP00000507269.1:n.-8G= | |
ENST00000684657.1:c.-8G= | ENSP00000507961.1:n.-8G= | |
ENST00000279146.8:c.-8G= MANE Select | ENSP00000279146.3:n.-8G= | |
ENST00000279146.7:c.-8G= | ENSP00000279146.3:n.-8G= | |
ENST00000528641.6:c.-8G= | ENSP00000434982.2:n.-8G= | |
ENST00000529797.1:n.103G= | ||
NM_001302960.1:c.-8G= | NP_001289889.1:n.-8G= | |
NM_003977.3:c.-8G= | NP_003968.3:n.-8G= | |
XM_024448761.1:c.-8G= | XP_024304529.1:n.-8G= | |
NM_003977.4:c.-8G= MANE Select | NP_003968.3:n.-8G= | |
NM_001302960.2:c.-8G= | NP_001289889.1:n.-8G= |