HGVS | Genome Assembly |
---|---|
NC_000014.9:g.99609366C>T , CM000676.2:g.99609366C>T | GRCh38 |
NC_000014.8:g.100075703C>T , CM000676.1:g.100075703C>T | GRCh37 |
NC_000014.7:g.99145456C>T | NCBI36 |
NG_051108.1:g.9891C>T |
HGVS | Amino-acid Change | |
---|---|---|
XM_006720277.2:c.-199+4751C>T | XP_006720340.1:n.-199+4751C>T | |
XM_011537236.1:c.-287+4751C>T | XP_011535538.1:n.-287+4751C>T | |
NM_001329411.1:c.-287+4751C>T | NP_001316340.1:n.-287+4751C>T | |
XM_006720277.3:c.-199+4751C>T | XP_006720340.1:n.-199+4751C>T | |
XM_011537236.2:c.-287+4751C>T | XP_011535538.1:n.-287+4751C>T | |
NM_001329411.2:c.-287+4751C>T | NP_001316340.1:n.-287+4751C>T |