HGVS | Genome Assembly |
---|---|
NC_000004.12:g.6269358T>G , CM000666.2:g.6269358T>G | GRCh38 |
NC_000004.11:g.6271085T>G , CM000666.1:g.6271085T>G | GRCh37 |
NC_000004.10:g.6321986T>G | NCBI36 |
NG_011700.1:g.4509T>G |
HGVS | Amino-acid change | |
---|---|---|
XM_017008586.1:c.4+7719T>G | XP_016864075.1:n.4+7719T>G |