HGVS | Genome Assembly |
---|---|
NC_000006.12:g.29946069T>A , CM000668.2:g.29946069T>A | GRCh38 |
NC_000006.11:g.29913846T>A , CM000668.1:g.29913846T>A | GRCh37 |
NC_000006.10:g.30021825T>A | NCBI36 |
NG_029217.2:g.8605T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000706901.1:c.*614T>A | ENSP00000516612.1:n.*614T>A | |
ENST00000706902.1:c.1093+788T>A | ENSP00000516613.1:n.1093+788T>A | |
ENST00000706903.1:c.*124+490T>A | ENSP00000516614.1:n.*124+490T>A | |
ENST00000706904.1:c.1093+788T>A | ENSP00000516615.1:n.1093+788T>A | |
ENST00000706905.1:c.*614T>A | ENSP00000516616.1:n.*614T>A |