HGVS | Genome Assembly |
---|---|
NC_000006.12:g.43769906C>T , CM000668.2:g.43769906C>T | GRCh38 |
NC_000006.11:g.43737643C>T , CM000668.1:g.43737643C>T | GRCh37 |
NC_000006.10:g.43845621C>T | NCBI36 |
NG_008732.1:g.4691C>T |
HGVS | Amino-acid Change | |
---|---|---|
NM_001318876.2:c.945+240635C>T | NP_001305805.1:n.945+240635C>T |