HGVS | Genome Assembly |
---|---|
NC_000004.12:g.6269353C>T , CM000666.2:g.6269353C>T | GRCh38 |
NC_000004.11:g.6271080C>T , CM000666.1:g.6271080C>T | GRCh37 |
NC_000004.10:g.6321981C>T | NCBI36 |
NG_011700.1:g.4504C>T |
HGVS | Amino-acid change | |
---|---|---|
XM_017008586.1:c.4+7714C>T | XP_016864075.1:n.4+7714C>T |