HGVS | Genome Assembly |
---|---|
NC_000004.12:g.6269519T>G , CM000666.2:g.6269519T>G | GRCh38 |
NC_000004.11:g.6271246T>G , CM000666.1:g.6271246T>G | GRCh37 |
NC_000004.10:g.6322147T>G | NCBI36 |
NG_011700.1:g.4670T>G |
HGVS | Amino-acid Change | |
---|---|---|
XM_017008586.1:c.4+7880T>G | XP_016864075.1:n.4+7880T>G |