HGVS | Genome Assembly |
---|---|
NC_000006.12:g.147796282T>C , CM000668.2:g.147796282T>C | GRCh38 |
NC_000006.11:g.148117418T>C , CM000668.1:g.148117418T>C | GRCh37 |
NC_000006.10:g.148159111T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
XM_017010850.1:c.460-151190T>C | XP_016866339.1:n.460-151190T>C |