HGVS | Genome Assembly |
---|---|
NC_000006.12:g.29946143G= , CM000668.2:g.29946143G= | GRCh38 |
NC_000006.11:g.29913920G= , CM000668.1:g.29913920G= | GRCh37 |
NC_000006.10:g.30021899G= | NCBI36 |
NG_029217.2:g.8679G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000706901.1:c.*688G= | ENSP00000516612.1:n.*688G= | |
ENST00000706902.1:c.1093+862G= | ENSP00000516613.1:n.1093+862G= | |
ENST00000706903.1:c.*124+564G= | ENSP00000516614.1:n.*124+564G= | |
ENST00000706904.1:c.1093+862G= | ENSP00000516615.1:n.1093+862G= | |
ENST00000706905.1:c.*688G= | ENSP00000516616.1:n.*688G= |