HGVS | Genome Assembly |
---|---|
NC_000014.9:g.99609558C>G , CM000676.2:g.99609558C>G | GRCh38 |
NC_000014.8:g.100075895C>G , CM000676.1:g.100075895C>G | GRCh37 |
NC_000014.7:g.99145648C>G | NCBI36 |
NG_051108.1:g.10083C>G |
HGVS | Amino-acid Change | |
---|---|---|
XM_006720277.2:c.-199+4943C>G | XP_006720340.1:n.-199+4943C>G | |
XM_011537236.1:c.-287+4943C>G | XP_011535538.1:n.-287+4943C>G | |
NM_001329411.1:c.-287+4943C>G | NP_001316340.1:n.-287+4943C>G | |
XM_006720277.3:c.-199+4943C>G | XP_006720340.1:n.-199+4943C>G | |
XM_011537236.2:c.-287+4943C>G | XP_011535538.1:n.-287+4943C>G | |
NM_001329411.2:c.-287+4943C>G | NP_001316340.1:n.-287+4943C>G |