HGVS | Genome Assembly |
---|---|
NC_000002.12:g.47617366A>G , CM000664.2:g.47617366A>G | GRCh38 |
NC_000002.11:g.47844505A>G , CM000664.1:g.47844505A>G | GRCh37 |
NC_000002.10:g.47698009A>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000644092.1:c.*1242+9785A>G | ENSP00000496351.1:n.*1242+9785A>G | |
ENST00000645339.1:c.2753-15436A>G | ENSP00000496441.1:n.2753-15436A>G | |
ENST00000646415.1:c.*125+9785A>G | ENSP00000495543.1:n.*125+9785A>G | |
XR_001738747.2:n.3004+9785A>G |