HGVS | Genome Assembly |
---|---|
NC_000006.12:g.147796126C>T , CM000668.2:g.147796126C>T | GRCh38 |
NC_000006.11:g.148117262C>T , CM000668.1:g.148117262C>T | GRCh37 |
NC_000006.10:g.148158955C>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
XM_017010850.1:c.460-151346C>T | XP_016866339.1:n.460-151346C>T |