HGVS | Genome Assembly |
---|---|
NC_000015.10:g.80152534T>G , CM000677.2:g.80152534T>G | GRCh38 |
NC_000015.9:g.80444876T>G , CM000677.1:g.80444876T>G | GRCh37 |
NC_000015.8:g.78231931T>G | NCBI36 |
NG_012833.1:g.4536T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000558022.5:c.-41T>G | ENSP00000453152.1:n.-41T>G |